Reagents and methods for sequencing

ABSTRACT

The disclosure provides a plurality of nucleic acid sequences comprising multiple variants of a reference sequence. The disclosure further provides plasmids, cells, methods and kits comprising the same.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of application Ser. No. 14/461,306,filed Aug. 15, 2014, which claims priority to U.S. provisionalapplication No. 61/903,268, filed Nov. 12, 2013, all of which areincorporated herein by reference in their entirety.

SEQUENCE LISTING

The instant application contains a Sequence Listing, which has beensubmitted electronically in ASCII format and is hereby incorporated byreference in its entirety. The Sequence Listing, labeled“059545.000016_SequenceListing_May2019_ST25.txt,” was created on May 30,2019, and is 7 KB.

BACKGROUND OF THE INVENTION

A significant challenge facing testing laboratories is quality control.Some reports have indicated that mutations in cancer genes werecorrectly identified by only 70% of testing laboratories (Bellon, et al.External Quality Assessment for KRAS Testing Is Needed: Setup of aEuropean Program and Report of the First Joined Regional QualityAssessment Rounds. Oncologist. 2011 April; 16(4): 467-478). Questionshave been raised regarding how to monitor next generation sequencing andassays as well as the concordance of variant calls across multipleplatforms, library preparation methods, and bioinformatic pipelines.Compositions and methods providing a flexible, single reagentrepresenting a large number of genetic variants are desired by those ofordinary skill in the art and are described herein.

SUMMARY OF THE INVENTION

The disclosure provides compositions, controls, plasmids, cells, methodsand kits comprising nucleic acid molecules.

In one embodiment, a nucleic acid molecule comprising multiple variantsof a reference is disclosed. In other embodiments, a mixture orcombination of nucleic acid molecules comprising variants of thereference sequence are disclosed.

In certain embodiments, the nucleic acid molecule or mixture of nucleicacid molecules comprise one or more variants present at a high orlow-frequency.

In certain embodiments, the disclosure provides a control reagentcomprising multiple nucleic acid molecules.

In yet another embodiment, a kit comprising at least one nucleic acidmolecule or mixture of nucleic acid molecules comprising variants isdisclosed

In another embodiment, a method for confirming the validity of asequencing reaction is disclosed. The method comprises including a knownnumber of representative sequences and/or variants thereof in a mixturecomprising a test sample potentially comprising a test nucleic acidsequence, and sequencing the nucleic acids in the mixture, whereindetection of all of the representative sequences and/or variants in themixture indicates the sequencing reaction was accurate.

The disclosure also provides a composition comprising multiple nucleicacid species wherein the nucleic acid sequence of each species differsfrom its neighbor species by a predetermined percentage.

In certain embodiments, a method is provided that comprises sequencing anucleic acid species in order to calibrate a sequencing instrument.

In yet other embodiments, the disclosure provides plasmids and cellsencoding the nucleic acids or mixture of nucleic acids disclosed herein.

The disclosure also provides a plasmid and/or a cell comprising multiplenucleic acid species wherein the nucleic acid sequence of each speciesdiffers from its neighbor species by a predetermined percentage.

The disclosure further provides a frequency ladder. The frequency laddercomprises a plurality of variants at different frequencies.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Exemplary EGFR amplicon selection.

FIG. 2 is a graph showing variant frequency at each nucleotide positionas well as percentage A and G content. Sequences 1-5 are the same andare used to dilute out sequences 6-10. Each sequence is found in its owncassette, and all cassettes are found in the same plasmid. This designprovides an absolute truth—e.g., there is 10% sequence 6 in this design.In contrast to mixing with genomic sequence, this provides the mostprecision when making a 10% mix. This could be used to calibrate assays.

FIG. 3 is a schematic of an exemplary plasmid with 10 sequences andrestriction sites, leading to equal ratios of each sequence.

FIG. 4 is a graph showing the frequency percentage per run comprisingPanel A (FLT3, PDGFRA, FGFR3, CSF1R, EGFR, HRAS, and TP53).

FIG. 5 is a graph showing the frequency percentage per run of Panel Aand Panel B (TP53, PIK3CA, GNA11, VHL, FBXW7, RET, HNF1A, and STK11)

FIG. 6 is a graph showing the frequency percentage per run of Panel A,Panel B, and Panel C (RB1, EGFR, ABL1, ERBB2, and ATM).

FIG. 7 is a graph showing the frequency percentage per run of Panel A,Panel B, Panel C, and Line D, which represents the number of reads(i.e., coverage)

FIG. 8 is a graph showing the number of variants (deletions, insertions,complex, multiple nucleotide variants (MNV), and single nucleotidevariants (SNV)) and average number of variants detected across multiplesites using CHPv2 (AMPLISEQ™ Cancer Hotspot Panel version 2),TSACP(TRUSEQ™ Amplicon Cancer Panel), and TSTP (TRUSIGHT™ Tumor Panel).

FIG. 9 is a graph showing analysis conducted with data from sites thattested two lots of the control at least once or one lot at least twice.Detection is indicated in dark squares and absence light squares.

FIG. 10 is a graph showing the mean number and mean percentage SNPsdetected for CHPv2 and TTP.

FIG. 11 is a graph showing the mean number and mean percentage of SNPsdetected for CHPv2 and TACP.

DETAILED DESCRIPTION OF THE INVENTION

Provided herein are compositions, methods, kits, plasmids, and cellscomprising nucleic acid reference sequences and variants of a referencesequence. The compositions disclosed herein have a variety of uses,including but not limited to, assay optimization, validation, andcalibration; peer-to-peer comparison; training and PT/EQA, QCmonitoring, reagent QC, and system installation assessment.

There is a recognized need in the market for flexible, reliable controlmaterials for NGS testing (see Assuring the Next Quality ofNext-Generation Sequencing in Clinical Laboratory Practice; NextGeneration Sequencing: Standardization of Clinical Testing (Nex-SToCT)Working group Principles and Guidelines, Nature Biotechnology,doi:10.1038/nbt.2403; and ACMG Clinical laboratory standards for nextgeneration sequencing, American College of Medical Genetics andGenomics,doi: 10.1038/gim.2013.92). This disclosure provides suchcontrol materials.

This disclosure relates to control reagents representing referencesequences and/or variants thereof (e.g., mutations) that may be used forvarious purposes such as, for instance, assay validation/quality controlin sequencing reactions (e.g., next generation sequencing (NGS) assays).Traditional metrics used to characterize the quality of a sequencingreaction include, for instance, read length, minimum quality scores,percent target-mapped reads, percent pathogen-specific reads, percentunique reads, coverage levels, uniformity, percent of non-coveredtargeted bases and/or real-time error rate. Parameters that may affectquality include, for instance, the types and/or number of analytes beingmonitored (e.g., the types and number of polymorphisms (single ormultiple nucleotide polymorphisms (SNPs, MNPs)), insertions and/ordeletions, amplicons, assay contexts and/or limits of detection), sampletype (e.g., mammalian cells, infectious organism, sample source),commutability (e.g., validation across multiple technology platformsand/or types of screening panels being utilized), sample preparation(e.g., library preparation type/quality and/or type of sequencingreaction (e.g., run conditions, sequence context)), and/or otherparameters. Those of ordinary skill in the art realize, for instance,that the quality of such reactions may vary between laboratories due tosubtle differences in guidelines, the metrics and parameters mentionedabove, the reference standards used, and the fact that many NGStechnologies are highly complex and evolving. This disclosure providesquality control reagents that may be used in different laboratories,under different conditions, with different types of samples, and/oracross various technology platforms to confirm that that assays arebeing carried out correctly and that results from different laboratoriesmay be reliably compared to one another (e.g, that each is of suitablequality). In some embodiments, the problem of confirming the quality ofa sequencing reaction is solved using a multiplex control comprisingmultiple nucleic acid fragments, each representing a different variantof a reference sequence.

In certain embodiments, a control reagent for use in sequencingreactions is provided. The control reagent may comprise one or morecomponents that may be used alone or combined to assess the quality of aparticular reaction. For instance, some assays are carried out toidentify genetic variants present within a biological sample. Thecontrol reagents described herein may also provide users with theability to compare results between laboratories, across technologyplatforms, and/or with different sample types. For instance, in someembodiments, the control reagent may represent a large number of lowpercentage (e.g., low frequency) variants of different cancer-relatedgenes that could be used to detect many low percentage variants in asingle assay and/or confirm the reliability of an assay. The controlreagent could be used to generate numerous data points to comparereactions (e.g., run-to-run comparisons). The control reagent may beused to determine the reproducibility of variant detection over timeacross multiple variables. The control reagent may be used to assess thequality of a sequencing run (i.e., that the instrument has sufficientsensitivity to detect the included variants at the given frequencies).The control reagent may also be used to differentiate between aproficient and a non-proficient user by comparing their sequencing runs,and/or to differentiate the quality of reagents between different lots.The control reagent may also aid in assay validation studies, as manyvariants are combined in one sample material. This obviates the need formultiple samples containing one or two variants each, and greatlyshortens the work and time required to validate the assay.

The control reagent typically comprises one or more nucleic acid (e.g.,DNA, RNA, circular RNA, hairpin DNA and/or RNA) fragments containing adefined reference sequence of a reference genome (defined as chromosomeand nucleotide range) and/or one or more variants of the referencesequence. The source material for the variants may be genomic DNA,synthetic DNA, and combinations thereof. A variant typically includesnucleotide sequence variations relative to the reference sequence. Thevariant and reference sequence typically share at least 50% or about75-100% (e.g., any of about 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85,86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99%) sequenceidentity. In some embodiments, however, the identity shared may besignificantly less where, for example, the variant represents a deletionor insertion mutation (either of which may be up to several kilobases ormore). An exemplary deletion may be, for instance, recurrent 3.8 kbdeletion involving exons 17a and 17b within the CFTR gene as describedby Tang, et al. (J. Cystic Fibrosis, 12(3): 290-294 (2013) (describing ac.2988+1616_c.3367+356de13796ins62 change, flanked by a pair ofperfectly inverted repeats of 32 nucleotides)). In some embodiments,variants may include at least one of a single nucleotide polymorphism(SNP), one or more multiple nucleotide polymorphism(s) (MNV),insertion(s), deletion(s), copy number variation(s), gene fusion(s),duplication(s), inversion(s), repeat polymorphism(s), homopolymer(s),non-human sequence(s), or any combination thereof. Such variants (whichmay include by reference any combinations) may be included in a controlreagent as part of the same or different components. The referencesequence(s) and/or variants may be arranged within a control reagent ascassettes.

Cassettes contains a reference sequence or variant adjoined and/oroperably linked to one or more restriction enzyme site(s), sequencingprimer(s) site, and/or hairpin-forming site(s). In some embodiments, itmay be useful to include different types of sequences adjacent to eachcassette; for instance, it may be useful to design one cassette to beadjacent to a restriction enzyme and/or a hairpin sequence. Doing so mayhelp prevent problems such as cross-amplification between adjacentfragments/cassettes. As such, each reference sequence and/or variant maybe releasable and/or detectable separate from any other referencesequence and/or variant. The typical cassette may be about 400 bp inlength but may vary between 50-20,000 bp (e.g., such as about any of 50,100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 2000, 3000, 4000,5000, 6000, 7000, 800, 900, 1000, 2500, 5000, 7500, 10000, 12500, 15000,17500, or 20000 bp). Each control reagent may comprise one or morecassettes, each representing one or more reference sequence(s) and/orvariant(s) (e.g., each being referred to as a “control sequence”). Eachreference sequence and/or variant may be present in a control sequenceand/or control reagent at percentage of about any of 0.1% to 100% (e.g.,about any 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 2.5, 5, 7.5,10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95,or 100%). For instance, a control sequence or control reagent that is100% reference sequence or variant would be a reagent representing onlyone reference sequence or variant. Similarly, a control sequence orcontrol reagent comprising 50% of a variant would be a control reagentrepresenting only up to two reference sequences and/or variants. Theremaining percentage could consist of other sequences such as controlsequences and the like.

In certain embodiments a T7 or other promoter can be present upstream ofeach cassette. This allows for massively parallel transcription of manygene regions. This technique facilitates construction of a controlcontaining equivalent amounts of each target sequence. When there areequivalent amounts of many targets, ease of use of the control isincreased. For example, contamination in a control in a patient samplewould be easier to detect because all transcripts would show up in thecontaminated sample. It is highly unlikely for patient samples tocontain, e.g., a large number of fusion transcripts, such an assayresult would signal the user that that a contamination issue is present.This is in contrast to a situation in which only one transcript ispresent at a much higher abundance in a contaminated sample—which couldlead to the contaminant being mistaken for a true positive signal. Theability to construct a control with equivalent amounts of each targetsequence eliminates the potential for this type of error.

In certain embodiments, the reference sequence(s) and/or variants may beadjoined and/or operably linked to one or more different restrictionenzyme sites, sequencing primer site(s), and/or hairpin-forming sites.As described above, certain designs may be used to prevent problems suchas cross-amplification between reference sequences and/or variants. Insome embodiments, the control sequences and/or cassettes may optionallybe arranged such that the same are releasable from the control reagent.This may be accomplished by, for instance, including restriction enzyme(RE) sites at either end of the control sequence. A control reagent maytherefore be arranged as follows: RE site/control sequence/RE site. TheRE sites may be the same and/or different from one another. The RE sitesin one cassette may also be the same and/or different to those presentin any other cassette. As such, the control sequences may be releasedfrom the cassette as desired by the user by treating the controlsequence with one or more particular restriction enzymes.

In some embodiments, the control reagent may comprise multiplecomponents that may be used together. In certain embodiments, themultiple components comprise a first and a second component which may beplasmids comprising different control sequences and/or differentarrangements of the same control sequences. Thus, the components mayrepresent the same or different reference sequences and/or variants.Such components may be used together as a panel, for instance, such thata variety of reference sequences and/or variants may be assayedtogether. Where the reference sequences and/or variants are the same,each component may include those variants in different cassettearrangements and/or forms. In some embodiments, the multiple componentsmay comprise a first component representing one or more SNP variants anda second component representing one or more multiple nucleotidepolymorphism(s), insertion(s), deletion(s), copy number variation(s),gene fusion(s), duplication(s), inversion(s), repeat polymorphism(s),homopolymer(s), and/or non-human sequence(s). The components may be thesame or different types of nucleic acids such as plasmids, with eachcomprising the same or different variants of one or more referencesequences arranged as described herein or as may be otherwise determinedto be appropriate by one of ordinary skill in the art. In someembodiments, different types of plasmids may be combined to provide amulti-component control reagent representing many different referencesequences and/or variants.

Plasmids can be quantified by any known means. In one embodiment,quantitation of each plasmid is performed using a non-human ‘xeno’digital PCR target sequence. The exact copy number of the plasmid isdetermined. The exact copy number of genomic DNA is also determined(obtained by quantification of genomic target site(s)). With thisinformation, controls can be accuratley and reproducibly developed thatcontain all targets/variants within a tight frequency range.

The variants may be contained within the control reagent as DNAfragments, each containing a defined sequence derived from a referencegenome (defined as chromosome and nucleotide range) with one or morevariations (e.g., nucleotide differences) introduced into the fragment.A variant may be, for instance, a sequence having one or more nucleotidesequence differences from the defined sequence (e.g., a referencesequence). For instance, an exemplary reference sequence may comprise“hostpots” suitable for modification. Such hotspots may representnucleotides and/or positions in a reference sequence that occur innature (e.g., mutations observed in cancer cells). One or more of suchhotspots may be modified by changing one or more nucleotides therein toproduce a control sequence (or portion thereof) that may be incorporatedinto a control reagent. For example, modification of the exemplaryepidermal growth factor receptor (EGFR) Ex19 reference sequence toproduce control sequences (Hotspots 1, 2, 3, 4, 5) is shown below (seealso, FIG. 1):

Wild Type (e.g., EGFR Ex19) CCAAGCTC (SEQ ID NO: 1) . . . AGGATCTTGA(SEQ ID NO: 2) . . . AACTGAATTC (SEQ ID NO: 3) . . . AAAAAG (SEQ ID NO:4) . . . ATCAAAGTGC (SEQ ID NO: 5) (400 bp)

Hotspot ID 1 CCAATCTC (SEQ ID NO: 6) . . . AGGATCTTGA (SEQ ID NO: 2) . .. AACTGAATTC (SEQ ID NO: 3) . . . AAAAAG (SEQ ID NO: 4) . . . ATCAAAGTGC(SEQ ID NO: 5)

Control Sequence Contains Multiple Hotspots

CCAATCTC (SEQ ID NO: 6; HOTSPOT ID 1) . . . AGGAACTTGA (SEQ ID NO: 7;HOTSPOT ID 2) . . . AACTCAATTC (SEQ ID NO: 8; HOTSPOT ID 3) . . . ATAAAG(SEQ ID NO: 9; HOTSPOT ID 4) . . . ATGAAAGTGC (SEQ ID NO: 10; HOTSPOT ID5). This exemplary control sequence thereby represents multiple EGFRvariants (e.g., Hotspot IDs 1, 2, 3, 4, 5, etc.) A control reagent maycomprise multiple control sequences, each representing one or morevariants of the same or different reference sequences. Any number ofvariants may be represented by a control sequence, and any number ofcontrol sequences may be included in a control reagent. A controlreagent may comprise, for instance, a number of variants such that theall possible variants of a particular reference sequence are representedby a single control reagent. For instance, the control reagent maycomprise multiple SNPs, MNPs, deletions, insertions and the like, eachrepresenting a different variant of the reference sequence. Additional,exemplary, non-limiting variants are shown in Tables 1A and 1B and Table6.

Control reagents may also be designed to represent multiple types ofcontrol sequences. For instance, control reagents may be designed thatrepresent multiple types of reference sequences and/or variants thereof(which may be found in control sequences alone or in combination).Exemplary categories of control sequences for which the control reagentsdescribed herein could have relevance include not only theaforementioned cancer-related areas but also fields of inheriteddisease, microbiology (e.g., with respect to antibiotic resistancemutations, immune-escape related mutations), agriculture (e.g. plantmicrobe and/or drug resistance-related mutations), livestock (e.g.,mutations related to particular livestock traits), food and watertesting, and other areas. Exemplary combinations (e.g., panels) ofcancer-related reference sequences that may be represented by aparticular control reagent (or combinations thereof) are shown in Table2.

The control reagents and methods for using the same described herein mayprovide consistent control materials for training, proficiency testingand quality control monitoring. For instance, the control reagents maybe used to confirm that an assay is functioning properly by including aspecific number of representative sequences and/or variants thereof thatshould be detected in an assay and then calculating the number that wereactually detected. This is exemplified by the data presented in Table 3:

As illustrated in Table 3, a “bad run” is identified where the number ofvariants detected does not match the number of variants expected to bedetected (e.g., included in the assay). As shown in the exemplary assayof Table 3, if a particular control reagent (or combination thereof)used in an assay includes 15 representative sequences and/or variantsthereof, all 15 should be detected if the assay is properly carried out.If less than 15 of these control sequences are not detected, the assayis identified as inaccurate (e.g., a “Bad Run”). If all 15 of thesequences are detected, the assay is identified as accurate (e.g., a“Good Run”). Variations of this concept are also contemplated herein, aswould be understood by those of ordinary skill in the art.

In certain embodiments, the control reagent may be prepared by mixingvariant DNA fragments (e.g., as may be incorporated into a plasmid) withgenomic DNA or synthesized DNA comprising “wild-type” (e.g.,non-variant) sequence. Such sequence may be obtained from or present incontrol cells (e.g., naturally occurring or engineered/cultured celllines). In some embodiments, the wild-type sequence may be included on aDNA fragment along with the variant sequence, or the variant sequencesmay be transfected into and/or mixed with cells (e.g., control cells).In certain embodiments, such mixtures may be used to prepareformalin-fixed, paraffin-embedded (FFPE) samples (e.g., control FFPEsamples), for example. For instance, in some embodiments, the controlreagent may be prepared and tested by designing a control sequence(e.g., an amplicon) comprising a representative sequence and/or variantthereof; designing restriction sites to surround each amplicon;synthesizing a nucleic acid molecule comprising a cassette comprisingthe amplicon and the restriction sites; and, incorporating the cassetteinto a plasmid backbone. The construct may then be tested by sequencingit alone (e.g, providing an expected frequency of 100%) or after mixingthe same with, for example, genomic DNA at particular expectedfrequencies (e.g., 50%). Such constructs may also be mixed with cellsfor various uses, including as FFPE controls.

In certain embodiments, the control reagents described herein can alsobe used to provide a frequency ladder. A frequency ladder is composed ofmany variants at different frequencies. In some embodiments, the controlreagent could be used to provide an “ladder” in, for example, 5%increments of abundance (e.g., about any of 1, 5, 10, 15, 20, 25, 30,35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 100% abundance).For example, the ladder could be constructed by taking a single samplewith many different variants present at high (e.g., 80% allelefrequency) and making dilutions down to low frequencies. Alternatively,the ladder could be a single sample containing variants at differentfrequencies. The ladder could be used as a reference for many sampletypes, including somatic variants at low abundance (e.g., tumor singlenucleotide polymorphisms), or germline variants present at, as anon-limiting example, about 50% abundance. Such a ladder may also beused to determine instrument limits of detection for many differentvariants at the same time. This saves users time in finding materialscontaining one to a few variants and resources for testing because allvariants are present in a single sample rather than many. An example isprovided in Table 8:

As shown in Table 8, a ladder was constructed by diluting a samplecontaining 555 variants starting at approximately 50% frequency down to˜3% frequency. The ladder was tested in duplicate using the IonAMPLISEQ® Cancer Hotspot Panel v2 using the Ion Torrent PERSONAL GENOMEMACHINE® (PGM). The frequencies for 35 of the variants are reported foreach sample tested. The shaded cells indicate that the variant was notdetected. Such data could be used to establish the limit of detectionfor each variant.

The ladder could be used across many platforms, including Sangersequencing and next generation platforms, and both RUO and IVDapplications could benefit from use of this standard. The frequencyladder could also serve as internal controls in sequencing reactions,much like the 1 kb DNA ladder serves as a reference in almost everyagarose gel. As an example, one design would provide five unique andfive identical sequences as shown in FIGS. 2 and 3. As shown therein, inone sequence position, there is a variant present in only one of theseten sequences. At a second position, the variant is present in two ofthe ten sequences. At the third position, the variant is present inthree of the sequences, and so on. This would yield variants at 10%frequency increments from 0-100%. This is a simplified example andrandom intervening sequences may be necessary to prevent sequencingartifacts. The product could take any suitable form such as anoligonucleotide (e.g., PCR fragment or synthetic oligonucleotide),plasmids, or one plasmid with concatenated sequences separated byidentical restriction enzyme sites (FIG. 3). An advantage of having allsequence variants on one plasmid is that the relative levels of all tensequences within a mixture would be well controlled; duringmanufacturing, the plasmid could be cleaved between each sequence withthe same enzyme, giving rise to ten fragments at equal ratios. As wouldbe understood by those of ordinary skill in the art, derivations of sucha ladder could include different variant types (e.g., insertions and/ordeletions), every nucleotide change could be incorporated into thedesign (e.g., A→C, A→T, etc.), and/or smaller increments could providefine-tuned measurement at abundances lower than 10%. For instance, asecond plasmid with other mutations could be added to the initialplasmid at a one to nine ratio, yielding variants at even lowerfrequencies. Such a low frequency sequencing ladder could be anessential control when measuring somatic mutations that appear, forexample, at <10% abundance. In some embodiments, such a sequencingladder may comprise multiple nucleic acid species wherein the nucleicacid sequence of each species differs from its neighbor species by apredetermined percentage (e.g., about any of 1, 2, 3, 4, 5, 6, 7, 8, 9,10% or more). Each species may comprise, for instance, any suitablenumber of nucleotides (e.g., about any of 5, 10, 20, 40, 50, 60, 70, 80,90, 100, 125, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375, 400,425, 450, 475, or 500). Each species may also comprise a homopolymersequence of at least 3 nucleotides. In some embodiments, the nucleicacid of the species is DNA, and these may be encoded on vectors such asplasmids and/or by and/or within cells. In some embodiments, eachspecies may comprise a nucleic acid bar code that may be unique to eachspecies. Methods comprising sequencing the nucleic acid species tocalibrate a sequencing instrument, to obtain data for sequencinginstrument development work, including algorithm development, basecalling, variant calling, and/or verify that an instrument isfunctioning properly (e.g., IQ/OQ/PQ) are also contemplated.

One of ordinary skill in the art would understand that the controlreagents described herein are broadly useful in a variety of sequencingsystems and/or platforms. For instance, the control reagents describedherein may be used in any type of sequencing procedure including but notlimited to Ion Torrent semiconductor sequencing, Illumina MISEQ®,capillary electrophoresis, microsphere-based systems (e.g., Luminex),Roche 454 system, DNA replication-based systems (e.g., SMRT by PacificBiosciences), nanoball- and/or probe-anchor ligation-based systems(Complete Genomics), nanopore-based systems and/or any other suitablesystem.

One of ordinary skill in the art would also understand that the controlreagents described herein are broadly useful in a variety of nucleicacid amplification-based systems and/or platforms. The control reagentsdescribed herein may used in and/or with any in vitro system formultiplying the copies of a target sequence of nucleic acid, as may beascertained by one of ordinary skill in the art. Such systems mayinclude, for instance, linear, logarithmic, and/or any otheramplification method including both polymerase-mediated amplificationreactions (such as polymerase chain reaction (PCR), helicase-dependentamplification (HDA), recombinase-polymerase amplification (RPA), androlling chain amplification (RCA)), as well as ligase-mediatedamplification reactions (such as ligase detection reaction (LDR), ligasechain reaction (LCR), and gap-versions of each), and combinations ofnucleic acid amplification reactions such as LDR and PCR (see, forexample, U.S. Pat. No. 6,797,470). Such systems and/or platforms maytherefore include, for instance, PCR (U.S. Pat. Nos. 4,683,202;4,683,195; 4,965,188; and/or 5,035,996), isothermal procedures (usingone or more RNA polymerases (see, e.g., PCT Publication No. WO2006/081222)), strand displacement (see, e.g., U.S. Pat. No. RE39007E),partial destruction of primer molecules (see, e.g., PCT Publication No.WO 2006/087574)), ligase chain reaction (LCR) (see, e.g., Wu, et al.,Genomics 4: 560-569 (1990)), and/or Barany, et al. Proc. Natl. Acad.Sci. USA 88:189-193 (1991)), Qβ RNA replicase systems (see, e.g., PCTPublication No. WO 1994/016108), RNA transcription-based systems (e.g.,TAS, 3SR), rolling circle amplification (RCA) (see, e.g., U.S. Pat. No.5,854,033; U.S. Patent Application Publication No. 2004/265897; Lizardiet al. Nat. Genet. 19: 225-232 (1998); and/or Bailer et al. Nucleic AcidRes., 26: 5073-5078 (1998)), and/or strand displacement amplification(SDA) (Little, et al. Clin. Chem. 45:777-784 (1999)), among others.These systems, along with the many other systems available to theskilled artisan, may be suitable for use with the control reagentsdescribed herein.

In one embodiment, a control reagent may be designed and tested usingone or more of the steps below:

-   -   designing a control sequence (e.g., an amplicon) comprising a        representative sequence of a particular gene of interest and/or        variants thereof (e.g., those targeted by commercially-available        NGS tests such as the AMPLISEQ Cancer Hotspot Panel v2, and/or        the TRUSEQ Amplicon Cancer Panel);    -   identifying sequence from a genome reference source (e.g.,        Genome Reference Consortium Human Reference 37 (GRCh37))        encompassing the amplicon;    -   designing a cassette comprising an ˜400 bp sequence comprising        the amplicon surrounded by (e.g., 5′ and 3′) the genomic        sequence identified in step b);    -   designing restriction sites to surround each cassette prepared        in step c) (e.g., where one version may additionally include        sequences that create a hairpin when the DNA is        single-stranded);    -   synthesizing a nucleic acid molecule comprising the cassette of        step c) and restriction sites of step d) using a common vector        (e.g., pUC57) (e.g., “plasmid V1”);    -   preparing a second plasmid (e.g., “plasmid V2”) comprising        multiple fragments of the gene of interest (and/or variants        thereof) with a hairpin structure and a restriction site between        each region;    -   optionally, linearizing the variant sequences contained within        plasmids V1 and/or V2 with a restriction enzyme;    -   mixing the variants with genomic DNA (e.g., wild-type gDNA) at a        particular expected variant frequency (e.g., approximately 50%);    -   optionally, testing the “variant sequence” alone (e.g.,        providing an expected variant frequency of 100%);    -   performing variant detection using NGS.

In certain embodiment, individual cassettes can be synthesized for allgenes of interest and combined with wild type. In certain embodiments, acassette can be designed with a plurality of variants, which do notinterfere with the detection of variants near or adjacent thereto.

In some embodiments, NGS may be performed using the Ion Personal GenomeMachine (PGM) by first constructing libraries following the user manualsfor the Ion AMPLISEQ® Library Preparation Manual with AMPLISEQ® CancerHotspot Panel v2 reagents; preparing template-positive Ion sphereparticles (ISPs) and enriching the same using the Ion OneTouch2instrument following the Ion PGM Template OT2 200 Kit Manual; sequencingusing the Ion PGM Sequencing 200 Kit v2 Manual or Sequencing on theIllumina MISEQ® following the TRUSEQ® Amplicon Cancer Panel user manualor the Illumina MiSeq® user manual; and, performing data analysis forPGM using the Torrent Variant Caller v3.4 and v3.6, and for MISEQ® usingthe MISEQ® Reporter v2.3).

The reagents and methods described herein may be used in a variety ofsettings with a variety of samples. For instance, these reagents andmethods may be used to analyze biological samples such as serum, wholeblood, saliva, tissue, urine, dried blood on filter paper (e.g, fornewborn screening), nasal samples, stool samples or the like obtainedfrom a patient and/or preparations thereof (e.g., FFPE preparations). Insome embodiments, control preparations comprising the control reagentsdescribed herein may be provided.

This disclosure further relates to kits comprising one or more controlreagents described herein. The kits may be used to carry out the methodsdescribed herein or others available to those of ordinary skill in theart along with, optionally, instructions for use. A kit may include, forinstance, control sequence(s) including multiple reference sequencesand/or variations thereof in the form of, for instance, one or moreplasmids. In some embodiments, the kit may contain a combination ofcontrol sequences organized to provide controls for many variations ofone or more reference sequences. In some embodiments, the variations mayrelate to an oncogene that is diagnostic for a particular cancer. Insome embodiments, for instance, the kit may comprise control reagentsand/or control samples (e.g., tissue samples) known to cover the breadthof mutations known for a particular cancer. In some embodiments, thevariations of the marker are variations of a mutation in a gene that areprognostic for the usefulness of treating with a drug. In someembodiments, the marker or markers are for a particular disease and/or avariety of diseases (e.g., cancer, infectious disease). In someembodiments, the control reagent(s) may be included in a test toascertain the efficacy of a drug in testing for the presence of adisease and/or progression thereof. In some embodiments, the kit maycomprise control reagents for testing for a series of diseases that havecommon characteristics and/or symptoms (e.g., related diseases). In someembodiments, the marker may have unknown significance but may otherwisebe of interest to the user (e.g., for basic research purposes). The kitmay also include a container (e.g., vial, test tube, flask, bottle,syringe or other packaging system (e.g., include injection orblow-molded plastic containers) into which one or more control reagentsmay be placed/contained, and in some embodiments, aliquoted). Where morethan one component is included in the kit, it will generally include atleast one second, third or other additional container into which theadditional components can be separately placed. Various combinations ofcomponents may also be packaged in a single container. The kits may alsoinclude reagent containers in close confinement for commercial sale.When the components of the kit are provided in one and/or more liquidsolutions, the liquid solution comprises an aqueous solution that may bea sterile aqueous solution. As mentioned above, the kit may also includeinstructions for employing the kit components as well as the use of anyother reagent not included in the kit. Instructions may includevariations that may optionally be implemented. The instructions may beprovided as a separate part of the kit (e.g., a paper or plastic insertor attachment) or as an internet-based application. In some embodiments,the kit may control reagents relating to between any number of referencesequences and/or variants thereof which may be detected alone or incombination with one another (e.g., a multiplex assay). In someembodiments, the kit may also comprise at least one other samplecontaining a defined amount of control reagent and “control” test celladmixed such that the same may provide a reference point for the user.Kits may further comprise one or more of a polymerase and/or one or moreoligonucleotide primers. Other variations and arrangements for the kitsof this disclosure are contemplated as would be understood by those ofordinary skill in the art.

Thus, in some embodiments, the disclosure provides a nucleic acidmolecule or mixture of nucleic acid molecules comprising multiplevariants of a reference sequence, each variant sequence may optionallybe releasable from the nucleic acid molecule. In certain embodiments,the nucleic acid molecule or mixture of nucleic acid molecules comprisesvariants releasable from the nucleic acid molecule using a restrictionenzyme.

In some embodiments, the nucleic acid molecule or mixture of nucleicacid molecules comprises at least one single nucleotide polymorphism(SNP), multiple nucleotide polymorphisms (MNP), insertion, deletion,copy number variation, gene fusion, duplication, inversion, repeatpolymorphism, homopolymer of a reference sequence, and/or a non-humansequence. In some embodiments, the nucleic acid molecule or mixture ofnucleic acid molecules comprises at least 5 variants. In certainembodiments, at least 15, 20, 30, 50, 100, 200, 300 400, 700, 1000variants are present. In yet other embodiments, greater than 1000variants are present. In some embodiments, each variant is present(e.g., in the sample being tested) at a high or low-frequency. Forinstance, in certain embodiments, each variant may be present at afrequency of 1%, 5%, 10%, 15%, 20%, 30%, 40% or 50% or more. In otherembodiments, each variant may be present at a frequency of less than50%, less than 40%, less than 20%, less than 15%, less than 10%, lessthan 5%, less than 3%, less than 1%, less than 0.5%, less than 0.1%, andany integer in between.

An advantage of the disclosed control materials is that the “truth” of asample is known. There are currently no reference materials for whichabsolute frequency (i.e, the truth) is known, that is, the actualfrequency of a given variant or combination of variants present are notknown. In contrast, in the disclosed control materials, the actualfrequency of variants is known.

Attendant to the teachings of this disclosure, standardized controlmaterials for next generation sequencing (NGS) assays can be produced.Issues such as variant call differences between sites, variability ofreagents across instruments, variation introduced by diversebioinformatics pipelines and filters, run-to-run and lab-to-labvariability can be identified and resolved and/or obviated utilizing thecontrol materials.

A further advantage is that the control materials disclosed herein cancomprise any number and type of variants, including insertions anddeletions of differing lengths, large numbers of SNPs, etc. No othercontrol material exists that provide such diversity.

The variants can be any of interest. There is no limit provided hereinwith respect to the type and number of variants that can be utilized inthe current disclosure.

In certain embodiments, modified nucleotides can be utilized asvariants. In certain embodiments, methylation can be detected. Forexample, CpG methylation can be utilized as a biomarker variant.

This disclosure also provides reagents and methods for confirming thevalidity of a sequencing reaction by including a known number ofrepresentative sequences and/or variants thereof in a mixture comprisinga test sample potentially comprising a test nucleic acid sequence andsequencing the nucleic acids in the mixture, wherein detection of all ofthe representative sequences and/or variants in the mixture indicatesthe sequencing reaction was accurate. The representative sequencesand/or variants may be of the type described herein. Compositionscomprising the same are also provided. The pre-determined percentage maybe, for instance, about 1, 5 or 10%. And each species may be from, forinstance, 20-500 nucleotides. Each species may comprise a homopolymersequence of at least 3 nucleotides. The nucleic acids may be DNA. Eachspecies may possess a nucleic acid barcode that may be unique to eachspecies. The nucleic acid species described herein may be used tocalibrate a sequencing instrument, for instance. Kits comprising suchspecies, optionally further comprising one or more polymerases and/orone or more oligonucleotide primers are also provided. Plasmids and/orcells comprising multiple nucleic acid species wherein the nucleic acidsequence of each species differs from its neighbor species by apredetermined percentage are also provided.

It is to be understood that the descriptions of this disclosure areexemplary and explanatory only and are not intended to limit the scopeof the current teachings. In this application, the use of the singularincludes the plural unless specifically stated otherwise. Also, the useof “comprise”, “contain”, and “include”, or modifications of those rootwords, for example but not limited to, “comprises”, “contained”, and“including”, are not intended to be limiting. Use of “or” means “and/or”unless stated otherwise. The term “and/or” means that the terms beforeand after can be taken together or separately. For illustrationpurposes, but not as a limitation, “X and/or Y” can mean “X” or “Y” or“X and Y”. Whenever a range of values is provided herein, the range ismeant to include the starting value and the ending value and any valueor value range therebetween unless otherwise specifically stated. Forexample, “from 0.2 to 0.5” may mean 0.2, 0.3, 0.4, and 0.5; rangestherebetween such as 0.2-0.3, 0.3-0.4, 0.2-0.4; increments there betweensuch as 0.25, 0.35, 0.225, 0.335, 0.49; increment ranges there betweensuch as 0.26-0.39; and the like. The term “about” or “approximately” mayrefer the ordinary meaning of the term but may also indicate a value orvalues within about any of 1-10 percent of the listed value.

The section headings used herein are for organizational purposes onlyand are not to be construed as limiting the subject matter described inany way. All literature and similar materials cited in this applicationincluding, but not limited to, patents, patent applications, articles,books, treatises, and internet web pages, regardless of the format ofsuch literature and similar materials, are expressly incorporated byreference in their entirety for any purpose. In the event that one ormore of the incorporated literature and similar materials defines oruses a term in such a way that it contradicts that term's definition inthis application, this application controls. While the present teachingsare described in conjunction with various embodiments, it is notintended that the present teachings be limited to such embodiments. Onthe contrary, the present teachings encompass various alternatives,modifications, and equivalents, as will be appreciated by those of skillin the art. Certain embodiments are further described in the followingexamples. These embodiments are provided as examples only and are notintended to limit the scope of the claims in any way.

Aspects of this disclosure may be further understood in light of thefollowing examples, which should not be construed as limiting the scopeof the disclosure in any way.

EXAMPLES Example 1

An exemplary control reagent was prepared and tested as described below:

a) amplicons were designed comprising the fragments shown in Tables 1-3;

b) genomic sequences were selected to encompass each amplicon (theselected genomic sequences being the chromosome and nucleotide positionsof the reference genome corresponding to the 5′ nucleotide of theforward and reverse primers for each amplicon and all the sequencebetween these two nucleotides);

c) a cassette was designed comprising an ˜400 bp EGFR sequencecomprising the amplicon surrounded by (e.g., 5′ and 3′) the genomicsequence identified in step b) (the reference sequence is added inroughly equally amounts to each end of the region defined in step b) tocomprise a ˜400 bp region);

d) restriction enzyme and other sites were designed to each cassetteprepared in step c) (e.g., where one version may additionally includesequences that create a hairpin when the DNA is single-stranded; therestriction enzymes being chosen such that the sequences of interest arenot digested but simply released from the control reagent) as shownbelow:

EGFR V1**

**EGFR_1, etc. represent EGFR variants; restriction enzyme sites forClaI, HindIII, SmaI, XhoI and Not I enzymes were positioned betweenvariants.

EGFR_1-ClaI-EGFR_2-HindIII-EGFR_3-SmaI-EGFR_4-XhoI-EGFR_5-NotI-EGFR_6/7-EGFR_8

EGFR V2***

***Hairpin 7 (HP(7)): GGGGGGGTTTTCCCCCCC (SEQ ID NO: 11);HindIII=HindIII RE site;

EGFR_4-HP(7)-ClaI-EGFR_5-HP(7)-HindIII-EGFR_6/7-HP(9)-Sma1-EGFR_8

Hairpin 9 (HP(9)): GGGGGGGGGAACCCCCCCCC (SEQ ID NO: 12); SmaI=SmaI REsite

e) the cassette of step d) was incorporated into a common vector (pUC57)(e.g., plasmid V1) by automated synthesis of oligonucleotides onsolid-phase synthesizers followed by ligation of overlappingoligonucleotides;

f) a second plasmid (e.g., “plasmid V2”) comprising multiple fragmentsof the gene of interest (and/or variants thereof) with a hairpinstructure and a restriction site between each region (e.g., as inexemplary construct EGFR V2 above and Table 4) was also prepared byautomated synthesis of oligonucleotides on solid-phase synthesizersfollowed by ligation of overlapping oligonucleotides;

g) the variant sequences (Tables 4-6) contained within plasmids V1and/or V2 were then linearized HindIII;

h) the variants were then mixed with genomic DNA (e.g., wild-type gDNA)at a particular expected variant frequency (e.g., approximately 50%)(plasmid DNA and human embryonic kidney (HEK-293) genomic DNA werequantified using a fluorometer (QUBIT®) to determine the concentration;plasmid and genomic DNA were then mixed together to obtain a 1:1molecular ratio (50% variant frequency));

i) the “variant sequences” were then tested alone to provide an expectedvariant frequency of 100%) to confirm sequencing; and,

j) variants of step h) were detected by NGS using the Ion PersonalGenome Machine (PGM) and Illumina MiSeq (results are presented in Table7).

Example 2 FFPE-Embedded Controls

The results of monitoring assays using FFPE-embedded controls arepresented in FIGS. 4-7. As shown therein, FFPE-embedded control reagentsmay be used to monitor variant detection, including low frequencyvariants (e.g., RB1 as indicated by “C” in the figures). Variants may betracked by the amplicon per se, GC content, sequence context, and/orvariant type as desired by those of ordinary skill in the art.

Each embodiment disclosed herein may be used or otherwise combined withany of the other embodiments disclosed. Any element of any embodimentmay be used in any embodiment. Although the invention has been describedwith reference to specific embodiments, it will be understood by thoseskilled in the art that various changes may be made and equivalents maybe substituted for elements thereof without departing from the truespirit and scope of the invention. In addition, modification may be madewithout departing from the essential teachings of the invention.

Example 3 555-Variant Control Performance Across Multiple Test Sites

A control sample was constructed that contained 555 variants from 53different genes and tested with the Ion AMPLISEQ® Cancer Hotspot Panelv2 (CHPv2), TRUSEQ® Amplicon Cancer Panel (TSACP) and the TRUSIGHT®Tumor Panel. For each panel, two lots of the AcroMetrix® OncologyHotspot Control were tested in duplicate, in at least two sites.Additional sites only tested one of the lots at least twice or both lotsonce. Sources of variation between sites may include differentinstruments, operators and general workflows. Also, variation inbioinformatics pipelines may have contributed significantly to variationin performance results.

FIG. 8 shows performance across different sites and panels. The averagenumber of variants of different types detected in the ACROMETRIX®Oncology Hotspot Control are reported by site and grouped by panel.Note: The total number of variants of each type is different for eachpanel. See FIGS. 8-11.

To assess the detection of specific variants across different panels,twenty-two clinically-relevant variants that were targeted by threepanels were selected. FIG. 9 shows detection of 22 selected variantsacross panels. Analysis was conducted with data from sites that testedtwo lots of the control at least once or one lot at least twice.Detection is indicated in dark squares and absence indicated in lightsquares. Site-to-site differences are apparent, even amongst thoseutilizing the same library preparation method, indicating the likelihoodof the bioinformatics pipeline having an impact on performance.

Example 4

Performance of the control material comprising 555 variants is shown inTable 9, wherein SNV (single nucleotide variant), MNV (multiplenucleotide variant), DEL (deletion), INS (insertion), for CHPv2(AMPLISEQ® Cancer Hotspot Panel v2), TSACP (TRUSEQ® Amplicon cancerpanel), and TSTP (TRUSIGHT® tumor panel) are shown. A variant wasconsidered to be covered by the test method if the variant waspositioned between the upstream and downstream primers. A variant wasconsidered detected if it was detected in at least one run of thecontrol. Sanger sequencing was performed on the synthetic DNA prior todilution with genomic DNA. Variants detected in the genomic DNA wereconfirmed using publicly available whole genome sequencing informationfor GM24385.

While preferred embodiments of the present invention have been shown anddescribed herein, it will be obvious to those skilled in the art thatsuch embodiments are provided by way of example only. Numerousvariations, changes, and substitutions will now occur to those skilledin the art without departing from the invention. It should be understoodthat various alternatives to the embodiments of the invention describedherein may be employed in practicing the invention. It is intended thatthe following claims define the scope of the invention and that methodsand structures within the scope of these claims and their equivalents becovered thereby.

TABLE 1A Exemplary Hotspot (HS) Variants Gene name Mutation ID MutationCDS Mutation Description Chr Start End MPL 27286 c.1514G > ASubstitution - Missense 1 43814979 43814979 MPL 18918 c.1544G > TSubstitution - Missense 1 43815009 43815009 MPL 27290 c.1555G > ASubstitution - Missense 1 43815020 43815020 NRAS 584 c.182A > GSubstitution - Missense 1 115256529 115256529 NRAS 1332933 c.174A > GSubstitution - coding silent 1 115256537 115256537 NRAS 577 c.52G > ASubstitution - Missense 1 115258730 115258730 NRAS 564 c.35G > ASubstitution - Missense 1 115258747 115258747 NRAS 24850 c.29G > ASubstitution - Missense 1 115258753 115258753 ALK 28056 c.3824G > ASubstitution - Missense 2 29432664 29432664 ALK 28055 c.3522C > ASubstitution - Missense 2 29443695 29443695 MSH6 13399 c.3246G > TSubstitution - coding silent 2 48030632 48030632 MSH6 13395 c.3261delCDeletion - Frameshift 2 48030647 48030647 MSH6 1021299 c.3300G > ASubstitution - coding silent 2 48030686 48030686 IDH1 28746 c.395G > ASubstitution - Missense 2 209113112 209113112 IDH1 1404902 c.388A > GSubstitution - Missense 2 209113119 209113119 IDH1 96922 c.367G > ASubstitution - Missense 2 209113140 209113140 ERBB4 48362 c.2791G > TSubstitution - Missense 2 212288954 212288955 ERBB4 169572 c.2782G > TSubstitution - Nonsense 2 212288963 212288964 ERBB4 232263 c.1835G > ASubstitution - Missense 2 212530083 212530084 ERBB4 573362 c.1828C > ASubstitution - Missense 2 212530090 212530091 ERBB4 1405173 c.1784A > GSubstitution - Missense 2 212530134 212530135 ERBB4 1614287 c.1089T > CSubstitution - coding silent 2 212576809 212576810 ERBB4 110095c.1022C > T Substitution - Missense 2 212576876 212576877 ERBB4 573356c.1003G > T Substitution - Missense 2 212576895 212576896 ERBB4 1405181c.909T > C Substitution - coding silent 2 212578347 212578348 ERBB4160825 c.885T > G Substitution - Missense 2 212578371 212578372 ERBB41015994 c.829C > A Substitution - Missense 2 212587171 212587172 ERBB41251447 c.804C > A Substitution - Nonsense 2 212587196 212587197 ERBB41405184 c.730A > G Substitution - Missense 2 212589811 212589812 ERBB4573353 c.704C > T Substitution - Missense 2 212589837 212589838 ERBB41015997 c.633G > A Substitution - coding silent 2 212589908 212589909ERBB4 48369 c.542A > G Substitution - Missense 2 212652763 212652764ERBB4 442267 c.515C > G Substitution - Missense 2 212652790 212652791VHL 14305 c.266T > A Substitution - Missense 3 10183797 10183797 VHL18080 c.277G > C Substitution - Missense 3 10183808 10183808 VHL 17658c.286C > T Substitution - Nonsense 3 10183817 10183817 VHL 17886c.296delC Deletion - Frameshift 3 10183827 10183827 VHL 17752 c.343C > ASubstitution - Missense 3 10188200 10188200 VHL 14312 c.353T > CSubstitution - Missense 3 10188210 10188210 VHL 14407 c.388G > CSubstitution - Missense 3 10188245 10188245 VHL 14412 c.431delGDeletion - Frameshift 3 10188288 10188288 VHL 17657 c.472C > GSubstitution - Missense 3 10191479 10191479 VHL 17612 c.481C > TSubstitution - Nonsense 3 10191488 10191488 VHL 14311 c.499C > TSubstitution - Missense 3 10191506 10191506 VHL 17837 c.506T > CSubstitution - Missense 3 10191513 10191513 MLH1 26085 c.1151T > ASubstitution - Missense 3 37067240 37067240 CTNNB1 5677 c.98C > GSubstitution - Missense 3 41266101 41266101 CTNNB1 5662 c.110C > TSubstitution - Missense 3 41266113 41266113 CTNNB1 5664 c.121A > GSubstitution - Missense 3 41266124 41266124 CTNNB1 5667 c.134C > TSubstitution - Missense 3 41266137 41266137 FOXL2 33661 c.402C > GSubstitution - Missense 3 138665163 138665163 PIK3CA 27495 c.35G > ASubstitution - Missense 3 178916648 178916648 PIK3CA 27376 c.93A > GSubstitution - Missense 3 178916706 178916706 PIK3CA 1420738 c.180A > GSubstitution - coding silent 3 178916793 178916793 PIK3CA 1041454c.210C > T Substitution - coding silent 3 178916823 178916823 PIK3CA27497 c.323G > A Substitution - Missense 3 178916936 178916936 PIK3CA13570 c.331A > G Substitution - Missense 3 178916944 178916944 PIK3CA125368 c.344G > T Substitution - Missense 3 178916957 178916957 PIK3CA1420774 c.536A > G Substitution - Missense 3 178917661 178917661 PIK3CA21462 c.971C > T Substitution - Missense 3 178921489 178921489 PIK3CA353193 c.1002C > T Substitution - coding silent 3 178921520 178921520PIK3CA 754 c.1035T > A Substitution - Missense 3 178921553 178921553PIK3CA 1420804 c.1213T > C Substitution - Missense 3 178927450 178927450PIK3CA 757 c.1258T > C Substitution - Missense 3 178927980 178927980PIK3CA 1420828 c.1370A > G Substitution - Missense 3 178928092 178928092PIK3CA 759 c.1616C > G Substitution - Missense 3 178936074 178936074PIK3CA 760 c.1624G > A Substitution - Missense 3 178936082 178936082PIK3CA 763 c.1633G > A Substitution - Missense 3 178936091 178936091PIK3CA 1420865 c.1640A > G Substitution - Missense 3 178936098 178936098PIK3CA 778 c.2102A > C Substitution - Missense 3 178938860 178938860PIK3CA 769 c.2702G > T Substitution - Missense 3 178947827 178947827PIK3CA 770 c.2725T > C Substitution - Missense 3 178947850 178947850PIK3CA 328026 c.3110A > G Substitution - Missense 3 178952055 178952055PIK3CA 775 c.3140A > G Substitution - Missense 3 178952085 178952085PIK3CA 12464 c.3204₋ 3205insA Insertion - Frameshift 3 178952149178952150 FGFR3 715 c.746C > G Substitution - Missense 4 1803568 1803568FGFR3 29446 c.753C > T Substitution - coding silent 4 1803575 1803575FGFR3 723 c.850delC Deletion - Frameshift 4 1803672 1803672 FGFR3 716c.1108G > T Substitution - Missense 4 1806089 1806089 FGFR3 24842c.1138G > A Substitution - Missense 4 1806119 1806119 FGFR3 724c.1150T > C Substitution - Missense 4 1806131 1806131 FGFR3 721c.1172C > A Substitution - Missense 4 1806153 1806153 FGFR3 1428724c.1928A > G Substitution - Missense 4 1807869 1807869 FGFR3 719c.1948A > G Substitution - Missense 4 1807889 1807889 FGFR3 24802c.2089G > T Substitution - Missense 4 1808331 1808331 PDGFRA 12418c.1698₋ 1712del15 Complex - deletion inframe 4 55141052 55141066 PDGFRA1430085 c.1743T > C Substitution - coding silent 4 55141097 55141097PDGFRA 22415 c.1977C > A Substitution - Missense 4 55144148 55144148PDGFRA 1430086 c.2001A > G Substitution - coding silent 4 5514417255144172 PDGFRA 743 c.2021C > T Substitution - Missense 4 5514454755144547 PDGFRA 587613 c.2517G > T Substitution - coding silent 455152085 55152085 PDGFRA 736 c.2525A > T Substitution - Missense 455152093 55152093 PDGFRA 28052 c.2544C > A Substitution - Missense 455152112 55152112 KIT 77973 c.92C > T Substitution - Missense 4 5556170255561702 KIT 1146 c.154G > A Substitution - Missense 4 55561764 55561764KIT 1430106 c.218A > G Substitution - Missense 4 55561828 55561828 KIT24637 c.1405T > C Substitution - Missense 4 55592081 55592081 KIT 41602c.1416A > G Substitution - coding silent 4 55592092 55592092 KIT 1326c.1509₋ 1510insG Insertion - In frame 4 55592185 55592186 CCTAT KIT96867 c.1516T > C Substitution - Missense 4 55592192 55592192 KIT 96885c.1526A > T Substitution - Missense 4 55592202 55592202 KIT 1430136c.1535A > G Substitution - Missense 4 55592211 55592211 KIT 1155c.1588G > A Substitution - Missense 4 55593431 55593431 KIT 1275c.1698C > T Substitution - coding silent 4 55593632 55593632 KIT 1290c.1727T > C Substitution - Missense 4 55593661 55593661 KIT 1299c.1755C > T Substitution - coding silent 4 55593689 55593689 KIT 1304c.1924A > G Substitution - Missense 4 55594221 55594221 KIT 12706c.1961T > C Substitution - Missense 4 55594258 55594258 KIT 36053c.2089C > T Substitution - Missense 4 55595599 55595599 KIT 1430171c.2148T > C Substitution - coding silent 4 55597500 55597500 KIT 21303c.2209G > A Substitution - Missense 4 55597561 55597561 KIT 20402c.2410C > T Substitution - Missense 4 55599284 55599284 KIT 19194c.2484 + 43T > A Unknown 4 55599401 55599401 KIT 133767 c.2558G > ASubstitution - Nonsense 4 55602737 55602737 KDR 35855 c.4008C > TSubstitution - coding silent 4 55946171 55946171 KDR 1430203 c.3433G > ASubstitution - Missense 4 55955112 55955112 KDR 48464 c.2917G > TSubstitution - Missense 4 55961023 55961023 KDR 1430212 c.2619A > GSubstitution - coding silent 4 55962505 55962505 KDR 32339 c.824G > TSubstitution - Missense 4 55979623 55979623 FBXW7 1427592 c.2079A > GSubstitution - coding silent 4 153244078 153244078 FBXW7 27083 c.2065C >T Substitution - Missense 4 153244092 153244092 FBXW7 732399 c.2033C > GSubstitution - Nonsense 4 153244124 153244124 FBXW7 34018 c.2001delGDeletion - Frameshift 4 153244156 153244156 FBXW7 27913 c.1580A > GSubstitution - Missense 4 153247222 153247222 FBXW7 30599 c.1576T > CSubstitution - Missense 4 153247226 153247226 FBXW7 30598 c.1558G > ASubstitution - Missense 4 153247244 153247244 FBXW7 34016 c.1451G > TSubstitution - Missense 4 153247351 153247351 FBXW7 22974 c.1436G > ASubstitution - Missense 4 153247366 153247366 FBXW7 22965 c.1394G > ASubstitution - Missense 4 153249384 153249384 FBXW7 22986 c.1338G > ASubstitution - Nonsense 4 153249440 153249440 FBXW7 161024 c.1322G > TSubstitution - Missense 4 153249456 153249456 FBXW7 22973 c.1177C > TSubstitution - Nonsense 4 153250883 153250883 FBXW7 22971 c.832C > TSubstitution - Nonsense 4 153258983 153258983 FBXW7 1052125 c.744G > TSubstitution - Missense 4 153259071 153259071 APC 18979 c.2543₋ 2544insAInsertion - Frameshift 5 112173834 112173835 APC 18852 c.2626C > TSubstitution - Nonsense 5 112173917 112173917 APC 19230 c.2639T > CSubstitution - Missense 5 112173930 112173930 APC 19330 c.2656C > TSubstitution - Nonsense 5 112173947 112173947 APC 19065 c.2752G > TSubstitution - Nonsense 5 112174043 112174043 APC 13872 c.3286C > TSubstitution - Nonsense 5 112174577 112174577 APC 1432250 c.3305A > GSubstitution - Missense 5 112174596 112174596 APC 1432260 c.3435A > GSubstitution - coding silent 5 112174726 112174726 APC 41617 c.3700delADeletion - Frameshift 5 112174991 112174991 APC 1432280 c.3795A > GSubstitution - coding silent 5 112175086 112175086 APC 19072 c.3871C > TSubstitution - Nonsense 5 112175162 112175162 APC 18960 c.3880C > TSubstitution - Nonsense 5 112175171 112175171 APC 18719 c.3923₋ 3924insAInsertion - Frameshift 5 112175214 112175215 APC 18702 c.3964G > TSubstitution - Nonsense 5 112175255 112175255 APC 19048 c.4057G > TSubstitution - Nonsense 5 112175348 112175348 APC 19652 c.4063T > CSubstitution - Missense 5 112175354 112175354 APC 18862 c.4132C > TSubstitution - Nonsense 5 112175423 112175423 APC 143913 c.4141C > TSubstitution - Missense 5 112175432 112175432 APC 18993 c.4189₋4190delGA Deletion - Frameshift 5 112175480 112175481 APC 19087c.4216C > T Substitution - Nonsense 5 112175507 112175507 APC 18836c.4285C > T Substitution - Nonsense 5 112175576 112175576 APC 13864c.4393₋ 4394delAG Deletion - Frameshift 5 112175684 112175685 APC1173082 c.4540delC Deletion - Frameshift 5 112175831 112175831 APC1183180 c.4561G > T Substitution - Nonsense 5 112175852 112175852 APC13879 c.4639G > T Substitution - Nonsense 5 112175930 112175930 APC41616 c.4654G > T Substitution - Nonsense 5 112175945 112175945 APC18561 c.4666₋ 4667insA Insertion - Frameshift 5 112175957 112175958 APC18875 c.4773₋ 4774insA Insertion - Frameshift 5 112176064 112176065 APC42906 c.4826C > T Substitution - Missense 5 112176117 112176117 CSF1R947 c.2906A > G Substitution - Missense 5 149433644 149433645 CSF1R310349 c.2878G > A Substitution - Missense 5 149433672 149433673 NPM117559 c.863₋ 864insTCTG Insertion - Frameshift 5 170837547 170837548EGFR 21683 c.323G > A Substitution - Missense 7 55211080 55211080 EGFR174732 c.340G > A Substitution - Missense 7 55211097 55211097 EGFR1451540 c.408C > T Substitution - coding silent 7 55211165 55211165 EGFR21687 c.866C > T Substitution - Missense 7 55221822 55221822 EGFR 43067c.874G > T Substitution - Missense 7 55221830 55221830 EGFR 21690c.1793G > T Substitution - Missense 7 55233043 55233043 EGFR 35825c.1859G > A Substitution - Missense 7 55233109 55233109 EGFR 13177c.2063T > C Substitution - Missense 7 55241615 55241615 EGFR 41905c.2092G > A Substitution - Missense 7 55241644 55241644 EGFR 6239c.2156G > C Substitution - Missense 7 55241708 55241708 EGFR 13979c.2170G > A Substitution - Missense 7 55241722 55241722 EGFR 53194c.2197C > T Substitution - Missense 7 55242427 55242427 EGFR 13182c.2203G > A Substitution - Missense 7 55242433 55242433 EGFR 17570c.2222C > T Substitution - Missense 7 55242452 55242452 EGFR 6223c.2235₋ 2249del15 Deletion - In frame 7 55242465 55242479 EGFR 28603c.2293G > A Substitution - Missense 7 55248995 55248995 EGFR 13190c.2375T > C Substitution - Missense 7 55249077 55249077 EGFR 12986c.2429G > A Substitution - Missense 7 55249131 55249131 EGFR 28610c.2441T > C Substitution - Missense 7 55249143 55249143 EGFR 53291c.2485G > A Substitution - Missense 7 55259427 55259427 EGFR 13424c.2497T > G Substitution - Missense 7 55259439 55259439 EGFR 6227c.2504A > T Substitution - Missense 7 55259446 55259446 EGFR 13430c.2515G > A Substitution - Missense 7 55259457 55259457 EGFR 6224c.2573T > G Substitution - Missense 7 55259515 55259515 EGFR 6213c.2582T > A Substitution - Missense 7 55259524 55259524 EGFR 14070c.2588G > A Substitution - Missense 7 55259530 55259530 EGFR 13008c.2612C > G Substitution - Missense 7 55259554 55259554 MET 706 c.504G >T Substitution - Missense 7 116339642 116339642 MET 710 c.1124A > GSubstitution - Missense 7 116340262 116340262 MET 29633 c.3082 + 1G > AUnknown 7 116412044 116412044 MET 1447462 c.3336T > C Substitution -coding silent 7 116417465 116417465 MET 697 c.3370C > G Substitution -Missense 7 116417499 116417499 MET 43064 c.3534G > C Substitution -Missense 7 116418969 116418969 MET 1214928 c.3562C > T Substitution -Nonsense 7 116418997 116418997 MET 1447471 c.3573T > C Substitution -coding silent 7 116419008 116419008 MET 1330154 c.3668T > GSubstitution - Missense 7 116422133 116422133 MET 700 c.3757T > GSubstitution - Missense 7 116423428 116423428 MET 48565 c.3778G > TSubstitution - Missense 7 116423449 116423449 MET 695 c.3785A > GSubstitution - Missense 7 116423456 116423456 MET 691 c.3803T > CSubstitution - Missense 7 116423474 116423474 SMO 13145 c.595C > TSubstitution - Missense 7 128845101 128845101 SMO 13147 c.970G > ASubstitution - Missense 7 128846040 128846040 SMO 216037 c.1234C > TSubstitution - Missense 7 128846398 128846398 SMO 13146 c.1604G > TSubstitution - Missense 7 128850341 128850341 SMO 13150 c.1918A > GSubstitution - Missense 7 128851593 128851593 BRAF 476 c.1799T > ASubstitution - Missense 7 140453136 140453136 BRAF 471 c.1790T > GSubstitution - Missense 7 140453145 140453145 BRAF 467 c.1781A > GSubstitution - Missense 7 140453154 140453154 BRAF 462 c.1742A > GSubstitution - Missense 7 140453193 140453193 BRAF 450 c.1391G > TSubstitution - Missense 7 140481417 140481417 BRAF 27986 c.1380A > GSubstitution - coding silent 7 140481428 140481428 BRAF 1448625c.1359T > C Substitution - coding silent 7 140481449 140481449 BRAF 6262c.1330C > T Substitution - Missense 7 140481478 140481478 EZH2 37028c.1937A > T Substitution - Missense 7 148508727 148508727 FGFR1 1292693c.816C > T Substitution - coding silent 8 38282147 38282147 FGFR1 187237c.448C > T Substitution - Missense 8 38285864 38285864 FGFR1 1456955c.421A > G Substitution - Missense 8 38285891 38285891 FGFR1 601c.374C > T Substitution - Missense 8 38285938 38285938 JAK2 12600c.1849G > T Substitution - Missense 9 5073770 5073770 JAK2 27063c.1860C > A Substitution - Missense 9 5073781 5073781 CDKN2A 12479c.358G > T Substitution - Nonsense 9 21971000 21971000 CDKN2A 12476c.341C > T Substitution - Missense 9 21971017 21971017 CDKN2A 12547c.330G > A Substitution - Nonsense 9 21971028 21971028 CDKN2A 13489c.322G > T Substitution - Missense 9 21971036 21971036 CDKN2A 12504c.247C > T Substitution - Missense 9 21971111 21971111 CDKN2A 12475c.238C > T Substitution - Nonsense 9 21971120 21971120 CDKN2A 13281c.205G > T Substitution - Nonsense 9 21971153 21971153 CDKN2A 12473c.172C > T Substitution - Nonsense 9 21971186 21971186 GNAQ 1110323c.1002C > T Substitution - coding silent 9 80336317 80336317 GNAQ 52975c.548G > A Substitution - Missense 9 80412493 80412493 GNAQ 1463119c.523A > T Substitution - Missense 9 80412518 80412518 ABL1 12631c.742C > G Substitution - Missense 9 133738342 133738342 ABL1 12577c.749G > A Substitution - Missense 9 133738349 133738349 ABL1 12576c.757T > C Substitution - Missense 9 133738357 133738357 ABL1 12573c.763G > A Substitution - Missense 9 133738363 133738363 ABL1 12602c.827A > G Substitution - Missense 9 133747520 133747520 ABL1 235737c.878₋ 879insGCC Complex - insertion inframe 9 133747571 133747572 ABL112578 c.1052T > C Substitution - Missense 9 133748391 133748391 ABL112611 c.1064A > G Substitution - Missense 9 133748403 133748403 ABL112605 c.1075T > G Substitution - Missense 9 133748414 133748414 ABL149071 c.1150C > A Substitution - Missense 9 133750319 133750319 ABL112604 c.1187A > G Substitution - Missense 9 133750356 133750356 NOTCH187862 c.7412C > A Substitution - Nonsense 9 139390779 139390779 NOTCH113070 c.7386delC Deletion - Frameshift 9 139390805 139390805 NOTCH112776 c.7375C > T Substitution - Nonsense 9 139390816 139390816 NOTCH113061 c.7318C > T Substitution - Nonsense 9 139390873 139390873 NOTCH113048 c.5033T > C Substitution - Missense 9 139397768 139397768 NOTCH1308587 c.5025C > T Substitution - coding silent 9 139397776 139397776NOTCH1 12771 c.4799T > C Substitution - Missense 9 139399344 139399344NOTCH1 13053 c.4793G > C Substitution - Missense 9 139399350 139399350NOTCH1 13042 c.4778T > C Substitution - Missense 9 139399365 139399365NOTCH1 12772 c.4721T > C Substitution - Missense 9 139399422 139399422RET 29803 c.1852T > C Substitution - Missense 10 43609096 43609096 RET29804 c.1858T > C Substitution - Missense 10 43609102 43609102 RET 1048c.1894₋ 1906 > AG Complex - deletion inframe 10 43609942 43609954 CT RET1223553 c.1942G > A Substitution - Missense 10 43609990 43609990 RET 976c.1991C > A Substitution - Missense 10 43610039 43610039 RET 21338c.2304G > C Substitution - Missense 10 43613840 43613840 RET 977 c.2647₋2648GC > Substitution - Missense 10 43615568 43615569 TT RET 963c.2701G > A Substitution - Missense 10 43615622 43615622 RET 965c.2753T > C Substitution - Missense 10 43617416 43617416 PTEN 5298c.19G > T Substitution - Nonsense 10 89624245 89624245 PTEN 5101 c.40A >G Substitution - Missense 10 89624266 89624266 PTEN 5153 c.49C > TSubstitution - Nonsense 10 89624275 89624275 PTEN 5107 c.71A > GSubstitution - Missense 10 89624297 89624297 PTEN 5134 c.80A > GSubstitution - Missense 10 89653782 89653782 PTEN 5142 c.112C > TSubstitution - Missense 10 89653814 89653814 PTEN 5050 c.142A > GSubstitution - Missense 10 89653844 89653844 PTEN 1349479 c.156T > CSubstitution - coding silent 10 89653858 89653858 PTEN 5129 c.163A > GSubstitution - Missense 10 89653865 89653865 PTEN 5257 c.166T > GSubstitution - Missense 10 89685271 89685271 PTEN 5036 c.202T > CSubstitution - Missense 10 89685307 89685307 PTEN 5916 c.209 + 5G > AUnknown 10 89685319 89685319 PTEN 5102 c.212G > A Substitution -Missense 10 89690805 89690805 PTEN 4956 c.227₋ 228delAT Deletion -Frameshift 10 89690820 89690821 PTEN 5205 c.245A > C Substitution -Missense 10 89690838 89690838 PTEN 5983 c.253 + 1G > A Unknown 1089690847 89690847 PTEN 5139 c.263A > G Substitution - Missense 1089692779 89692779 PTEN 5109 c.302T > C Substitution - Missense 1089692818 89692818 PTEN 5266 c.314G > T Substitution - Missense 1089692830 89692830 PTEN 5199 c.334C > G Substitution - Missense 1089692850 89692850 PTEN 5123 c.395G > A Substitution - Missense 1089692911 89692911 PTEN 5130 c.449A > G Substitution - Missense 1089692965 89692965 PTEN 5144 c.464A > G Substitution - Missense 1089692980 89692980 PTEN 5287 c.477G > T Substitution - Missense 1089692993 89692993 PTEN 5907 c.493-12delT Unknown 10 89711863 89711863PTEN 35406 c.578T > C Substitution - Missense 10 89711960 89711960 PTEN4978 c.595₋ 597delATG Deletion - In frame 10 89711977 89711979 PTEN 5279c.610C > A Substitution - Missense 10 89711992 89711992 PTEN 5072c.615G > A Substitution - Missense 10 89711997 89711997 PTEN 5154c.697C > T Substitution - Nonsense 10 89717672 89717672 PTEN 5292c.703G > T Substitution - Nonsense 10 89717678 89717678 PTEN 35849c.721T > C Substitution - Missense 10 89717696 89717696 PTEN 43075c.787A > T Substitution - Nonsense 10 89717762 89717762 PTEN 5809c.800delA Deletion - Frameshift 10 89717775 89717775 PTEN 1349606c.879A > G Substitution - coding silent 10 89720728 89720728 PTEN 5312c.895G > T Substitution - Nonsense 10 89720744 89720744 PTEN 4958 c.955₋958delACTT Deletion - Frameshift 10 89720804 89720807 PTEN 1349625c.1025A > G Substitution - Missense 10 89720874 89720874 PTEN 5966c.1027 − 2A > G Unknown 10 89725042 89725042 PTEN 4936 c.1040₋ 1041delTCDeletion - Frameshift 10 89725057 89725058 PTEN 1349633 c.1055A > GSubstitution - Missense 10 89725072 89725072 PTEN 23645 c.1091C > GSubstitution - Missense 10 89725108 89725108 FGFR2 36912 c.1647T > ASubstitution - Missense 10 123258034 123258034 FGFR2 36906 c.1144T > CSubstitution - Missense 10 123274774 123274774 FGFR2 36904 c.1124A > GSubstitution - Missense 10 123274794 123274794 FGFR2 1346272 c.1108A > GSubstitution - Missense 10 123274810 123274810 FGFR2 36901 c.929A > GSubstitution - Missense 10 123279503 123279503 FGFR2 29824 c.913G > ASubstitution - Missense 10 123279519 123279519 FGFR2 36903 c.755C > GSubstitution - Missense 10 123279677 123279677 HRAS 499 c.182A > GSubstitution - Missense 11 533874 533874 HRAS 495 c.175G > ASubstitution - Missense 11 533881 533881 HRAS 249860 c.81T > CSubstitution - coding silent 11 534242 534242 HRAS 483 c.35G > TSubstitution - Missense 11 534288 534288 ATM 21323 c.1009C > TSubstitution - Missense 11 108117798 108117798 ATM 21825 c.1229T > CSubstitution - Missense 11 108119823 108119823 ATM 22499 c.1810C > TSubstitution - Missense 11 108123551 108123551 ATM 1158828 c.1898 + 2T >A Unknown 11 108123641 108123641 ATM 21826 c.2572T > C Substitution -Missense 11 108138003 108138003 ATM 22507 c.3925G > A Substitution -Missense 11 108155132 108155132 ATM 21920 c.5044G > T Substitution -Missense 11 108170479 108170479 ATM 218294 c.5152C > G Substitution -Missense 11 108170587 108170587 ATM 49005 c.5178 − 1G > T Unknown 11108172374 108172374 ATM 172204 c.5188C > T Substitution - Nonsense 11108172385 108172385 ATM 21918 c.5224G > C Substitution - Missense 11108172421 108172421 ATM 12792 c.5380C > T Substitution - coding silent11 108173640 108173640 ATM 1183962 c.5476T > G Substitution - Missense11 108173736 108173736 ATM 21922 c.5821G > C Substitution - Missense 11108180945 108180945 ATM 12951 c.7325A > C Substitution - Missense 11108200958 108200958 ATM 12791 c.7996A > G Substitution - Missense 11108204681 108204681 ATM 21636 c.8084G > C Substitution - Missense 11108205769 108205769 ATM 1235404 c.8095C > A Substitution - Missense 11108205780 108205780 ATM 22481 c.8174A > T Substitution - Missense 11108206594 108206594 ATM 1183939 c.8624A > G Substitution - Missense 11108218045 108218045 ATM 22485 c.8668C > G Substitution - Missense 11108218089 108218089 ATM 21930 c.8839A > T Substitution - Missense 11108225590 108225590 ATM 21626 c.9023G > A Substitution - Missense 11108236087 108236087 ATM 1351060 c.9054A > G Substitution - coding silent11 108236118 108236118 ATM 21624 c.9139C > T Substitution - Nonsense 11108236203 108236203 KRAS 41307 c.491G > A Substitution - Missense 1225362805 25362805 KRAS 19940 c.351A > C Substitution - Missense 1225378647 25378647 KRAS 554 c.183A > C Substitution - Missense 1225380275 25380275 KRAS 546 c.175G > A Substitution - Missense 1225380283 25380283 KRAS 1169214 c.101C > T Substitution - Missense 1225398207 25398207 KRAS 14208 c.104C > T Substitution - Missense 1225398215 25398215 KRAS 521 c.35G > A Substitution - Missense 12 2539828425398284 KRAS 507 c.24A > G Substitution - coding silent 12 2539829525398295 PTPN11 13011 c.181G > T Substitution - Missense 12 112888165112888165 PTPN11 13013 c.205G > A Substitution - Missense 12 112888189112888189 PTPN11 13015 c.215C > T Substitution - Missense 12 112888199112888199 PTPN11 13000 c.226G > A Substitution - Missense 12 112888210112888210 PTPN11 13034 c.1472C > T Substitution - Missense 12 112926852112926852 PTPN11 13027 c.1508G > C Substitution - Missense 12 112926888112926888 PTPN11 1358900 c.1519A > G Substitution - Missense 12112926899 112926899 PTPN11 13031 c.1528C > A Substitution - Missense 12112926908 112926908 HNF1A 21471 c.617G > T Substitution - Missense 12121431413 121431413 HNF1A 24900 c.632A > C Substitution - Missense 12121431428 121431428 HNF1A 24832 c.685C > T Substitution - Nonsense 12121431481 121431481 HNF1A 21474 c.710A > G Substitution - Missense 12121431506 121431506 HNF1A 24923 c.779C > T Substitution - Missense 12121432032 121432032 HNF1A 24692 c.787C > T Substitution - Missense 12121432040 121432040 HNF1A 21481 c.872₋ 873insC Insertion - Frameshift 12121432125 121432126 FLT3 1166729 c.2516A > G Substitution - Missense 1328592629 28592629 FLT3 783 c.2503G > T Substitution - Missense 1328592642 28592642 FLT3 25248 c.2492G > A Substitution - Missense 1328592653 28592653 FLT3 786 c.2039C > T Substitution - Missense 1328602329 28602329 FLT3 27907 c.1800₋ 1801ins21 Insertion - In frame 1328608255 28608256 FLT3 19522 c.1775T > C Substitution - Missense 1328608281 28608281 FLT3 28042 c.1352C > T Substitution - Missense 1328610138 28610138 RB1 890 c.409G > T Substitution - Nonsense 13 4891924448919244 RB1 915 c.596T > A Substitution - Nonsense 13 48923148 48923148RB1 28816 c.940 − 2A > T Unknown 13 48941628 48941628 RB1 891 c.958C > TSubstitution - Nonsense 13 48941648 48941648 RB1 1367204 c.968A > GSubstitution - Missense 13 48941658 48941658 RB1 1367206 c.982A > GSubstitution - Missense 13 48941672 48941672 RB1 879 c.1072C > TSubstitution - Nonsense 13 48942685 48942685 RB1 895 c.1363C > TSubstitution - Nonsense 13 48953760 48953760 RB1 887 c.1654C > TSubstitution - Nonsense 13 48955538 48955538 RB1 888 c.1666C > TSubstitution - Nonsense 13 48955550 48955550 RB1 1367255 c.1687T > CSubstitution - Missense 13 48955571 48955571 RB1 892 c.1735C > TSubstitution - Nonsense 13 49027168 49027168 RB1 35483 c.1814 + 2T > CUnknown 13 49027249 49027249 RB1 870 c.2028₋ 2040del13 Deletion -Frameshift 13 49033891 49033903 RB1 13117 c.2053C > T Substitution -Nonsense 13 49033916 49033916 RB1 942 c.2063T > C Substitution -Missense 13 49033926 49033926 RB1 1042 c.2107 − 2A > G Unknown 1349037865 49037865 RB1 883 c.2117G > T Substitution - Missense 1349037877 49037877 RB1 940 c.2143A > T Substitution - Nonsense 1349037903 49037903 RB1 1367309 c.2153A > G Substitution - Missense 1349037913 49037913 RB1 868 c.2242G > T Substitution - Nonsense 1349039164 49039164 RB1 916 c.2261T > G Substitution - Missense 1349039183 49039183 RB1 551465 c.2267A > G Substitution - Missense 1349039189 49039189 RB1 254910 c.2293A > T Substitution - Nonsense 1349039215 49039215 AKT1 33765 c.49G > A Substitution - Missense 14105246551 105246551 IDH2 33733 c.515G > A Substitution - Missense 1590631838 90631838 IDH2 1375400 c.474A > G Substitution - coding silent15 90631879 90631879 IDH2 41590 c.419G > A Substitution - Missense 1590631934 90631934 CDH1 1379165 c.1058A > G Substitution - Missense 1668846087 68846087 CDH1 19748 c.1108G > C Substitution - Missense 1668846137 68846137 CDH1 19750 c.1204G > A Substitution - Missense 1668847282 68847282 CDH1 25267 c.1733₋ 1734insC Insertion - Frameshift 1668855925 68855926 CDH1 19746 c.1742T > C Substitution - Missense 1668855934 68855934 CDH1 19758 c.1774G > A Substitution - Missense 1668855966 68855966 CDH1 19743 c.1849G > A Substitution - Missense 1668856041 68856041 CDH1 19822 c.1901C > T Substitution - Missense 1668856093 68856093 CDH1 19418 c.1913G > A Substitution - Nonsense 1668856105 68856105 TP53 13747 c.1146delA Deletion - Frameshift 17 75729637572963 TP53 307348 c.1123C > T Substitution - Nonsense 17 75729867572986 TP53 1191161 c.1101 − 2A > G Unknown 17 7573010 7573010 TP5311073 c.1024C > T Substitution - Nonsense 17 7574003 7574003 TP53 11286c.1015G > T Substitution - Nonsense 17 7574012 7574012 TP53 11071c.1009C > T Substitution - Missense 17 7574018 7574018 TP53 11514c.1001G > T Substitution - Missense 17 7574026 7574026 TP53 11354c.991C > T Substitution - Nonsense 17 7576855 7576855 TP53 44823c.981T > G Substitution - Nonsense 17 7576865 7576865 TP53 46088c.963A > G Substitution - coding silent 17 7576883 7576883 TP53 10786c.949C > T Substitution - Nonsense 17 7576897 7576897 TP53 10663c.916C > T Substitution - Nonsense 17 7577022 7577022 TP53 10710c.892G > T Substitution - Nonsense 17 7577046 7577046 TP53 10863c.833C > T Substitution - Missense 17 7577105 7577105 TP53 10660c.818G > A Substitution - Missense 17 7577120 7577120 TP53 10662c.743G > A Substitution - Missense 17 7577538 7577538 TP53 6932 c.733G >A Substitution - Missense 17 7577548 7577548 TP53 10812 c.722C > TSubstitution - Missense 17 7577559 7577559 TP53 10725 c.701A > GSubstitution - Missense 17 7577580 7577580 TP53 10758 c.659A > GSubstitution - Missense 17 7578190 7578190 TP53 44317 c.653T > ASubstitution - Missense 17 7578196 7578196 TP53 10667 c.646G > ASubstitution - Missense 17 7578203 7578203 TP53 43947 c.614A > GSubstitution - Missense 17 7578235 7578235 TP53 10738 c.542G > ASubstitution - Missense 17 7578388 7578388 TP53 10808 c.488A > GSubstitution - Missense 17 7578442 7578442 TP53 10739 c.481G > ASubstitution - Missense 17 7578449 7578449 TP53 10670 c.469G > TSubstitution - Missense 17 7578461 7578461 TP53 10801 c.404G > ASubstitution - Missense 17 7578526 7578526 TP53 11582 c.395A > GSubstitution - Missense 17 7578535 7578535 TP53 11462 c.388C > GSubstitution - Missense 17 7578542 7578542 TP53 44226 c.380C > TSubstitution - Missense 17 7578550 7578550 TP53 44985 c.375 + 17G > AUnknown 17 7579295 7579295 TP53 43904 c.375G > A Substitution - codingsilent 17 7579312 7579312 TP53 10716 c.329G > T Substitution - Missense17 7579358 7579358 TP53 46103 c.319T > G Substitution - Missense 177579368 7579368 TP53 44492 c.273G > A Substitution - Nonsense 17 75794147579414 TP53 43910 c.245C > T Substitution - Missense 17 7579442 7579442TP53 12168 c.166G > T Substitution - Nonsense 17 7579521 7579521 TP5344907 c.151G > T Substitution - Nonsense 17 7579536 7579536 TP53 43664c.134T > C Substitution - Missense 17 7579553 7579553 TP53 46286c.112C > T Substitution - Nonsense 17 7579575 7579575 TP53 85573c.80delC Deletion - Frameshift 17 7579716 7579716 ERBB2 14060 c.2264T >C Substitution - Missense 17 37880220 37880220 ERBB2 1251412 c.2305G > TSubstitution - Missense 17 37880261 37880261 ERBB2 20959 c.2324₋2325ins12 Insertion - In frame 17 37880995 37880996 ERBB2 14065c.2524G > A Substitution - Missense 17 37881332 37881332 ERBB2 686c.2570A > G Substitution - Missense 17 37881378 37881378 ERBB2 21985c.2632C > T Substitution - Missense 17 37881440 37881440 SMAD4 1389031c.306T > C Substitution - coding silent 18 48575112 48575112 SMAD4 14229c.377T > C Substitution - Missense 18 48575183 48575183 SMAD4 218557c.389C > T Substitution - Missense 18 48575195 48575195 SMAD4 14168c.403C > T Substitution - Nonsense 18 48575209 48575209 SMAD4 13115c.431C > G Substitution - Nonsense 18 48575671 48575671 SMAD4 14118c.502G > T Substitution - Nonsense 18 48581198 48581198 SMAD4 1226725c.533C > A Substitution - Nonsense 18 48581229 48581229 SMAD4 308153c.547C > T Substitution - Nonsense 18 48581243 48581243 SMAD4 14057c.733C > T Substitution - Nonsense 18 48584560 48584560 SMAD4 22901c.766C > T Substitution - Nonsense 18 48584593 48584593 SMAD4 14217c.776₋ 777delCT Deletion - Frameshift 18 48584603 48584604 SMAD4 14163c.931C > T Substitution - Nonsense 18 48586262 48586262 SMAD4 14167c.955 + 5G > C Unknown 18 48586291 48586291 SMAD4 1389054 c.1001A > GSubstitution - Missense 18 48591838 48591838 SMAD4 1389057 c.1010A > GSubstitution - Missense 18 48591847 48591847 SMAD4 14109 c.1018A > GSubstitution - Missense 18 48591855 48591855 SMAD4 14111 c.1028C > GSubstitution - Nonsense 18 48591865 48591865 SMAD4 14249 c.1156G > CSubstitution - Missense 18 48593405 48593405 SMAD4 14103 c.1216G > ASubstitution - Missense 18 48593465 48593465 SMAD4 14223 c.1229₋1230insCA Insertion - Frameshift 18 48593478 48593479 SMAD4 1389077c.1248A > G Substitution - coding silent 18 48593497 48593497 SMAD414096 c.1333C > T Substitution - Nonsense 18 48603032 48603032 SMAD414114 c.1504A > G Substitution - Missense 18 48604682 48604682 SMAD41389099 c.1519A > G Substitution - Missense 18 48604697 48604697 SMAD414134 c.1576G > T Substitution - Nonsense 18 48604754 48604754 SMAD41389106 c.1591C > A Substitution - coding silent 18 48604769 48604769STK11 21212 c.169delG Deletion - Frameshift 19 1207077 1207077 STK1121570 c.465 − 1G > T Unknown 19 1220371 1220371 STK11 27316 c.475C > TSubstitution - Nonsense 19 1220382 1220382 STK11 20944 c.580G > TSubstitution - Missense 19 1220487 1220487 STK11 25229 c.595G > TSubstitution - Nonsense 19 1220502 1220502 STK11 29005 c.816C > TSubstitution - coding silent 19 1221293 1221293 STK11 21355 c.842C > TSubstitution - Missense 19 1221319 1221319 STK11 21360 c.1062C > GSubstitution - Missense 19 1223125 1223125 GNA11 21651 c.547C > TSubstitution - Missense 19 3115012 3115012 GNA11 52969 c.626A > TSubstitution - Missense 19 3118942 3118942 JAK3 34213 c.2164G > ASubstitution - Missense 19 17945696 17945696 JAK3 34214 c.1715C > TSubstitution - Missense 19 17948009 17948009 SRC 1227526 c.1460C > TSubstitution - Missense 20 36031630 36031631 GNAS 244725 c.489C > TSubstitution - coding silent 20 57480494 57480494 GNAS 27887 c.601C > TSubstitution - Missense 20 57484420 57484420 GNAS 27888 c.680A > TSubstitution - Missense 20 57484596 57484596 SMARCB1 1002 c.118C > TSubstitution - Nonsense 22 24133967 24133967 SMARCB1 991 c.141C > ASubstitution - Nonsense 22 24133990 24133990 SMARCB1 24595 c.157C > TSubstitution - Nonsense 22 24134006 24134006 SMARCB1 992 c.472C > TSubstitution - Nonsense 22 24143240 24143240 SMARCB1 51386 c.566₋567ins19 Insertion - Frameshift 22 24145547 24145548 SMARCB1 993c.601C > T Substitution - Nonsense 22 24145582 24145582 SMARCB1 999c.607G > A Substitution - Missense 22 24145588 24145588 SMARCB1 1057c.1148delC Deletion - Frameshift 22 24176357 24176357

TABLE 1B Exemplary Copy Number Variants (CNV) Gene Name Chromosome StartEnd ERBB2 chr17 37845134 37845207 ERBB2 chr17 37852282 37852381 ERBB2chr17 37860184 37860303 ERBB2 chr17 37871503 37871582 ERBB2 chr1737876682 37876784 ERBB2 chr17 37884464 37884584 ERBB2 chr17 3785490337855025 ERBB2 chr17 37884065 37884183 ERBB2 chr17 37866483 37866606ERBB2 chr17 37880963 37881086 KRAS chr12 25378600 25378682 PDGFRA chr455140973 55141093

TABLE 2 Control Reagent* Sequence A B C D E F G H 1 CSF1R APC APC APCAPC CSF1R APC APC 2 EGFR EGFR CSF1R CSF1R CSF1R EGFR EGFR CSF1R 3 FBXW7FBXW7 EGFR FGFR3 EGFR FGFR1 FGFR3 EGFR 4 FGFR3 FGFR3 ERBB4 FLT3 FBXW7FGFR3 FLT3 FGFR3 5 FLT3 FLT3 FGFR3 KDR FGFR3 FLT3 HRAS FLT3 6 GNA11 KDRFLT3 KRAS FLT3 HRAS IDH1 HRAS 7 HNF1A KRAS HRAS PDGFRA HRAS KDR KDR IDH18 HRAS PDGFRA KDR RET KRAS KIT KRAS KRAS 9 PDGFRA PIK3CA KIT STK11PDGFRA KRAS PDGFRA PDGFRA 10 PIK3CA RET KRAS TP53 RET MET RET PIK3CA 11RET TP53 PDGFRA — SMAD4 NOTCH1 TP53 RET 12 STK11 — RET — TP53 PDGFRA —STK11 13 TP53 — SMAD4 — — PIK3CA — TP53 14 VHL — TP53 — — SMARCB1 — — 15— — — — — SMO — — 16 — — — — — TP53 — — *APC (Adenomatous polyposiscoli, deleted in polyposis 2.5 (DP2.5); Chr. 5: 112.04-112.18 Mb; Ref.Seq. NM_000038 and NP_000029), CSF1R (Colony stimulating factor 1receptor, macrophage colony-stimulating factor receptor (M-CSFR), CD115;Chr. 5, 149.43-149.49 Mb; Ref. Seq. NM_005211 and NM_005202), EGFR(epidermal growth factor receptor; Chr. 7: 55.09-55.32 Mb; RefSeq Nos.NM_005228 and NP_0052219), FBXW7 (F-box/WD repeat-containing protein 7;Chr. 4: 153.24-153.46 Mb; RefSeq. Nos. NM_001013415 and NP_001013433),FGFR1 (Fibroblast growth factor receptor 1, basic fibroblast growthfactor receptor 1, fms-related tyrosine kinase-2/Pfeiffer syndrome,CD331; Chr. 8: 38.27-38.33 Mb; RefSeq. Nos. NM_001174063 andNP_001167534), FGFR3 (Fibroblast growth factor receptor 3, CD333; chr.4: 1.8-1.81 Mb; RefSeq Nos. NM_000142 and NP_000133), FLT3 (Fms-liketyrosine kinase 3, CD135, fetal liver kinase-2 (Flk2); Chr. 13:28.58-28.67 Mb; RefSeq Nos. NM_004119 and NP_004110), GNA11 (Guaninenucleotide-binding protein subunit alpha-11; Chr. 19: 3.09-3.12 Mb;RefSeq Nos. NM_002067 and NP_002058), HNF1A (hepatocyte nuclear factor 1homeobox A; Chr. 12: 121.42-121.44 Mb; RefSeq Nos. NM_000545 andNP_000536), HRAS (GTPase HRas, transforming protein p21; Chr. 11:0.53-0.54 Mb; RefSeq Nos. NM_001130442 and NP_001123914), IDH1(Isocitrate dehydrogenase 1 (NADP+), soluble; Chr. 2: 209.1-209.13 Mb;RefSeq Nos. NM_005896 and NP_005887), KDR (Kinase insert domainreceptor, vascular endothelial growth factor receptor 2, CD309; Chr. 4:55.94-55.99 Mb; RefSeq Nos. NM_002253 and NP_002244), KIT (Mast/stemcell growth factor receptor (SCFR), proto-oncogene c-Kit,tyrosine-protein kinase Kit, CD117; Chr. 4: 55.52-55.61 Mb; RefSeq Nos.NM_000222 and NP_000213), KRAS (GTPase KRas, V-Ki-ras2 Kirsten ratsarcoma viral oncogene homolog; Chr. 12: 25.36-25.4 Mb; RefSeq Nos.NM_004985-NP_004976), MET (c-Met, MNNG HOS Transforming gene, hepatocytegrowth factor receptor; Chr. 7: 116.31-116.44 Mb; RefSeq Nos. NM_000245and NP_000236), NOTCH1 (Notch homolog 1, translocation-associated(Drosophila); Chr. 9: 139.39-139.44; RefSeq Nos. NM_017617 andNP_060087), PDGFRA (Alpha-type platelet-derived growth factor receptor;Chr. 4: 55.1-55.16 Mb; RefSeq Nos. NM_006206 and NP_006197), PIK3CA(p110α protein; Chr. 3: 178.87-178.96 Mb; RefSeq Nos. NM_006218 andNP_006209), RET (receptor tyrosine kinase; Chr. 10: 43.57-43.64; RefSeqNos. NM_000323 and NP_065681), SMAD4 (Chr. 18: 48.49-48.61 Mb; RefSeqNos. NM_005359 and NP_005350), SMARCB1 (SWI/SNF-relatedmatrix-associated actin-dependent regulator of chromatin subfamily Bmember 1; Chr. 22: 24.13-24.18 Mb; RefSeq Nos. NM_001007468 andNP_001007469), SMO (Smoothened; Chr. 7: 128.83-128.85 Mb; RefSeq Nos.NM_005631 and NP_005622), STK11 (Serine/threonine kinase 11, liverkinase B1 (LKB1), renal carcinoma antigen NY-REN-19; Chr. 19: 1.19-1.23Mb; RefSeq Nos. NM_000455 and NP_000446), TP53 (protein 53, tumorprotein 53; Chr. 17: 7.57-7.59 Mb; RefSeq Nos. NM_000546 and NP_000537),VHL (Von Hippel-Lindau tumor suppressor; Chr. 3: 10.18-10.19 Mb; RefSeqNos. NM_000551 and NP_000542).

One or more variants of each of these reference sequences may also berepresented in each control sequence and/or control reagent. In someembodiments, for instance, multiple variants may be included for eachreference sequence. Panels of reference sequences may also be designedto represent particular metabolic, genetic information processing,environmental information processing, cellular process, organismalsystem, disease, drug development, or other pathways (e.g., KEGGpathways (http://www.genome.jp/kegg/pathway.html, Nov. 8, 2013)).Control reagents such as these may be assayed separately or combinedinto a single assay. The control reagents may also be designed toinclude various amounts of each reference sequences and/or variantsthereof.

TABLE 3 Number of Variants Number of Variants Run ID Detected ExpectedDetection Rate Bad Run 8 15 53% Bad Run 12 15 80% Good Run 15 15 100%Good Run 15 15 100% Good Run 15 15 100% Good Run 15 15 100% Good Run 1515 100% Good Run 15 15 100%

TABLE 4 Included in Plasmid Included in Plasmid Fragment ID # ofVariants V1 V2 EGFR_1 1 Yes No EGFR_2 2 Yes No EGFR_3 2 Yes No EGFR_4 13Yes Yes EGFR_5 7 Yes Yes EGFR_6/7 10 Yes Yes EGFR_8 8 Yes Yes

TABLE 5 Included variants for each EGFR fragment EGFR_1 EGFR_2 EGFR_3EGFR_4 EGFR_5 EGFR_6_7 EGFR_8 COSM21683 COSM21686 COSM21689 COSM41905COSM13180 COSM28603 COSM6224 COSM21687 COSM21690 COSM28508 COSM53194COSM26445 COSM12675 COSM28511 COSM18419 COSM6241 COSM6213 COSM12988COSM13182 COSM12376 COSM14070 COSM13427 COSM17570 COSM12381 COSM28607COSM41603 COSM6223 COSM13007 COSM33725 COSM28601 COSM21984 COSM6240COSM13008 COSM6252 COSM13192 COSM26438 COSM6239 COSM28610 COSM12373COSM41663 COSM22992 COSM28510 COSM13979

TABLE 6 Mutation Detail Muta- Gene Mutation Mutation GRCh37 tion ID nameID Mutation CDS Mutation AA Description Chr Start End strand 21683 EGFR21683 c.323G > A p.R108K Substitution - 7 55211080 55211080 + Missense21686 EGFR 21686 c.865G > A p.A289T Substitution - 7 55221821 55221821 +Missense 21687 EGFR 21687 c.866C > T p.A289V Substitution - 7 5522182255221822 + Missense 21689 EGFR 21689 c.1787C > T p.P596L Substitution -7 55233037 55233037 + Missense 21690 EGFR 21690 c.1793G > T p.G598VSubstitution - 7 55233043 55233043 + Missense 41905 EGFR 41905 c.2092G >A p.A698T Substitution - 7 55241644 55241644 + Missense 28508 EGFR 28508c.2104G > T p.A702S Substitution - 7 55241656 55241656 + Missense 28511EGFR 28511 c.2108T > C p.L703P Substitution - 7 55241660 55241660 +Missense 12988 EGFR 12988 c.2125G > A p.E709K Substitution - 7 5524167755241677 + Missense 13427 EGFR 13427 c.2126A > C p.E709A Substitution -7 55241678 55241678 + Missense 41603 EGFR 41603 c.2134T > C p.F712LSubstitution - 7 55241686 55241686 + Missense 28601 EGFR 28601 c.2135T >C p.F712S Substitution - 7 55241687 55241687 + Missense 6252 EGFR 6252c.2155G > A p.G719S Substitution - 7 55241707 55241707 + Missense 6239EGFR 6239 c.2156G > C p.G719A Substitution - 7 55241708 55241708 +Missense 12373 EGFR 12373 c.2159C > T p.S720F Substitution - 7 5524171155241711 + Missense 22992 EGFR 22992 c.2161G > A p.G721S Substitution -7 55241713 55241713 + Missense 28510 EGFR 28510 c.2162G > C p.G721ASubstitution - 7 55241714 55241714 + Missense 13979 EGFR 13979 c.2170G >A p.G724S Substitution - 7 55241722 55241722 + Missense 13180 EGFR 13180c.2188C > T p.L730F Substitution - 7 55242418 55242418 + Missense 53194EGFR 53194 c.2197C > T p.P733S Substitution - 7 55242427 55242427 +Missense 18419 EGFR 18419 c.2200G > A p.E734K Substitution - 7 5524243055242430 + Missense 13182 EGFR 13182 c.2203G > A p.G735S Substitution -7 55242433 55242433 + Missense 17570 EGFR 17570 c.2222C > T p.P741LSubstitution - 7 55242452 55242452 + Missense 6223 EGFR 6223c.2235_2249del15 p.E746_A750delELREA Deletion - 7 55242465 55242479 + Inframe 21984 EGFR 21984 c.2281G > T p.D761Y Substitution - 7 5524251155242511 + Missense 28603 EGFR 28603 c.2293G > A p.V765M Substitution -7 55248995 55248995 + Missense 26445 EGFR 26445 c.2300C > T p.A767VSubstitution - 7 55249002 55249002 + Missense 6241 EGFR 6241 c.2303G > Tp.S768I Substitution - 7 55249005 55249005 + Missense 12376 EGFR 12376c.2307_2308insGCCAGCGTG p.V769_D770insASV Insertion - 7 5524900955249010 + In frame 12381 EGFR 12381 c.2319_2320insAACCCCCACp.H773_V774insNPH Insertion - 7 55249021 55249022 + In frame 13007 EGFR13007 c.2335_2336GG > TT p.G779F Substitution - 7 55249037 55249038 +Missense 6240 EGFR 6240 c.2369C > T p.T790M Substitution - 7 5524907155249071 + Missense 13192 EGFR 13192 c.2428G > A p.G810S Substitution -7 55249130 55249130 + Missense 28610 EGFR 28610 c.2441T > C p.L814PSubstitution - 7 55249143 55249143 + Missense 41663 EGFR 41663 c.2462T >C p.I821T Substitution - 7 55249164 55249164 + Missense 6224 EGFR 6224c.2573T > G p.L858R Substitution - 7 55259515 55259515 + Missense 12675EGFR 12675 c.2575G > A p.A859T Substitution - 7 55259517 55259517 +Missense 6213 EGFR 6213 c.2582T > A p.L861Q Substitution - 7 5525952455259524 + Missense 14070 EGFR 14070 c.2588G > A p.G863D Substitution -7 55259530 55259530 + Missense 28607 EGFR 28607 c.2603A > G p.E868GSubstitution - 7 55259545 55259545 + Missense 33725 EGFR 33725 c.2609A >G p.H870R Substitution - 7 55259551 55259551 + Missense 13008 EGFR 13008c.2612C > G p.A871G Substitution - 7 55259554 55259554 + Missense 26438EGFR 26438 c.2620G > A p.G874S Substitution - 7 55259562 55259562 +Missense

TABLE 7 Results of EGFR plasmid EGFR Plasmid V1 EGFR Plasmid V2 MutationIon AmpliSeq Illumina Ion AmpliSeq Illumina ID CHP2 TruSeq CHP2 TruSeq21683 Called Called Not Included Not Included 21686 Called Called NotIncluded Not Included 21687 Called Called Not Included Not Included21689 Called Not Targeted Not Included Not Included 21690 Called CalledNot Included Not Included 41905 Called Not Called** Called Not Called**28508 Called Not Called** Called Not Called** 28511 Called Not Called**Called Not Called** 12988 Not Called Not Called** Not Called NotCalled** 13427 Called Not Called** Called Not Called** 41603 Called NotCalled** Called Not Called** 28601 Called Not Called** Called NotCalled** 6252 Called Not Called** Called Not Called** 6239 Called NotCalled** Called Not Called** 12373 Not Called Not Called** Not CalledNot Called** 22992 Called Not Called** Called Not Called** 28510 CalledNot Called** Called Not Called** 13979 Called Not Called** Called NotCalled** 13180 Called Called Called Called 53194 Called Called CalledCalled 18419 Called Called Called Called 13182 Called Called CalledCalled 17570 Called Called Called Called 6223 Not Called* Called NotCalled* Called 21984 Called Called Called Called 28603 Called CalledCalled Called 26445 Called Not Called Called Not Called 6241 Called NotCalled Called Not Called 12376 Called Not Called Called Not Called 12381Called Not Called Called Not Called 13007 Called Called Called Called6240 Called Called Called Called 13192 Called Called Called Called 28610Called Called Called Called 41663 Called Not Called Called Not Called6224 Called Not Called Called Not Called 12675 Called Not Called CalledNot Called 6213 Called Not Called Called Not Called 14070 Called NotCalled Called Not Called 28607 Called Not Called Called Not Called 33725Called Not Called Called Not Called 13008 Called Not Called Called NotCalled 26438 Called Not Called Called Not Called *Mutation not called bysoftware, but manual inspection revealed that the sequence correspondedto the correct mutation **Variant introduced in primer region of testmethod Called: sequence variant noted by analysis software Not Targeted:sequence variant not included in sequence analyzed by the test method

TABLE 8 Gene Mutation CDS Mutation AA Mutation 2.8 2.8 5.4 5.4 11.0 11.018.4 18.4 29.5 29.5 47.9 47.9 BRAF c. 1359T > C p. P453P SNP 4.7 8.8 714.3 15.5 24.3 27.4 39.4 39.3 59.8 58.3 EGFR c.340G > A p.E114K SNP 4.77.5 7.8 14.5 15.4 25.3 23.9 38.6 39.3 59 58.8 EGFR c.323G > A p.R108KSNP 5.1 7.8 7.9 15 14.8 26.7 25.3 40.4 39.3 59 59.2 BRAF c. 1380A > Gp.G460G SNP 4.8 8.7 7 14.9 15.5 24.2 27.4 39.3 39.2 59.5 57.8 EGFRc.874G > T p.V292L SNP 4.1 8.7 5.5 12.9 14.4 27.9 27.1 41.5 41.4 62.958.9 EGFR c.2235_2249del15 p.E746_A750delELREA DEL 18.3 16.8 26.2 27.741.4 43.6 61.2 59.5 KRAS c.111 + 1C > T p.? SNP 4.5 8 6.3 15.4 13.4 24.324.7 38.2 37.4 58.5 59.7 EGFR c.2429G > A p.G810D SNP 3.1 5.6 8.3 6.712.1 14.4 25.3 25.4 36.8 40 55.1 55.7 EGFR c.2612C > G p.A871G SNP 3.15.8 8 7.2 13.7 17.4 24.9 27.5 39.6 40.4 61.2 60.8 EGFR c.2208G > Ap.G735S SNP 3.4 4.7 7.8 8.5 15.9 16.2 24.8 29.6 39.8 43.5 57.9 60.7 EGRFc.2375T > C p.L792P SNP 3.9 4.2 8.6 5.7 14.6 14.5 22.1 27.2 39.2 41.1 5959.5 EGFR c.2170G > A p.G724S SNP 3.8 5 8.8 8.6 16.7 16.9 27.9 28.6 43.139.1 62 57.6 EGFR c.2588G > A p.G863D SNP 3.3 5.2 8 7.1 13.9 17.4 23.826.9 40.4 40.3 61.6 60.5 KRAS c.104C > T p.T35I SNP 3.9 3.7 7.8 6.9 15.413.6 24.4 25.8 38.5 37.4 57.7 59.8 EGFR c.2222C > T p.P741L SNP 3.2 4.67.8 7.9 16.2 16.5 25.8 28.1 41.4 43.5 59.1 60.2 KRAS c.351A > C p.K117NSNP 5.2 4.2 7.6 7.1 14.7 15.3 23 24.4 38.3 46.5 55.4 61.2 EGFR c.866C >T p.A289V SNP 3 4.2 9.3 5.6 12.8 14.6 27.9 27 44.2 41.4 62.9 57.6 EGFRc.1793G > T p.G598V SNP 4.2 5.5 7 6.6 14.3 16.1 23.6 24.7 38 41.8 54.858.3 EGFR c.2293G > A p.V765M SNP 3.9 4.3 8.8 5.5 14.6 14.3 223 27.639.3 40.8 58.9 59.9 EGFR c.2441T > C p.L814P SNP 3.1 6.6 9.3 6.8 12 16.226.1 25.8 37.5 41.5 55.6 58.7 EGFR c.2092G > A p.A698T SNP 3.7 5.2 9.18.9 16.6 17.1 28.2 28.8 41 38.5 62.5 58.5 BRAF c.1391G > T p.G464V SNP2.7 4.6 8.7 7 14.5 15.4 24.1 27 39.4 39.2 59.4 57.8 BRAF c.1742A > Gp.N581S SNP 3.7 4.9 8.9 8.2 12.4 25.1 28.6 39.3 43.9 59.4 57.2 BRAFc.1781A < G p.D594G SNP 4 4.8 8.3 8.4 12.3 25.7 28.4 39.7 43.8 58.2 57.2BRAF c.1790T > G p.L597T SNP 3.6 4.7 8.1 8.3 12.3 25.9 28.6 38.6 44 57.157.4 BRAF c.1799T > A p.V600E SNP 4 4.7 8.6 8.3 12.2 26.4 28.6 39 43.958 57.4 KRAS c.24A > G p.V8V SNP 4.7 3 8.3 6.7 14.8 13.2 25 24.3 37 36.756.2 59.1 KRAS c.35G > A p.G12D SNP 4.6 3.4 8.1 6.8 15.2 12.8 24.5 24.536 36.7 57.4 60 EGFR c.2197C > T p.P733S SNP 3.5 5.2 8 7.5 16 16.8 24.828.1 40.9 43.6 59 60.1 KRAS c.175G > A p.A59T SNP 4.5 4.4 8.3 6.5 15.614.2 24 26.4 38.1 40.9 58.6 60.7 KRAS c.183A > C p.Q61H SNP 4.5 4.5 7.57 15.5 14.3 23.2 26.9 40.3 40.8 60.5 61 EGFR c.2582T > A p.L861Q SNP 2.75.7 8.2 6.7 13.8 17.2 23.8 27.1 39.9 40.2 60.6 60.4 EGFR c.2573T > Gp.L858R SNP 2.7 5.3 8.4 7.1 13.8 17.1 22.9 26 39.8 40.1 60.7 60.6 EGFRc.2156G > C p.G719A SNP 3.6 5.4 9.3 8.4 16.6 16.5 27.9 29.3 42.5 38.762.4 57.8 BRAF c.1330C > T p.R444W SNP 2.9 4.5 8.6 6.7 14.5 15.6 24.427.9 38 39.2 60.2 59.3

TABLE 9 Chromosome Position Reference 1 43814979 G 1 43815009 G 143815020 G 1 115256529 T 1 115256537 T 1 115256669 G 1 115258730 C 1115258747 C 1 115258753 C 2 29432664 C 2 29443695 G 2 48030632 G 248030639 AC 2 48030686 G 2 48030838 A 2 209113112 C 2 209113119 T 2209113140 C 2 212288955 C 2 212288964 C 2 212530084 C 2 212530091 G 2212530135 T 2 212576810 A 2 212576877 G 2 212576896 C 2 212578348 A 2212578372 A 2 212587172 G 2 212587197 G 2 212589812 T 2 212589838 G 2212589909 C Chromosome Position Alternate 1 43814979 A 1 43815009 T 143815020 A 1 115256529 C 1 115256537 C 1 115256669 A 1 115258730 T 1115258747 T 1 115258753 T 2 29432664 T 2 29443695 T 2 48030632 T 248030639 A 2 48030686 A 2 48030838 T 2 209113112 T 2 209113119 C 2209113140 T 2 212288955 A 2 212288964 A 2 212530084 T 2 212530091 T 2212530135 C 2 212576810 G 2 212576877 A 2 212576896 A 2 212578348 G 2212578372 C 2 212587172 T 2 212587197 T 2 212589812 C 2 212589838 A 2212589909 T Chromosome Position Length Mutation ID Gene 1 43814979 1COSM27286 MPL 1 43815009 1 COSM18918 MPL 1 43815020 1 COSM27290 MPL 1115256529 1 COSM584 NRAS 1 115256537 1 COSM1332933 NRAS 1 115256669 1gDNA31 NRAS 1 115258730 1 COSM577 NRAS 1 115258747 1 COSM564 NRAS 1115258753 1 COSM24850 NRAS 2 29432664 1 COSM28056 ALK 2 29443695 1COSM28055 ALK 2 48030632 1 COSM13399 MSH6 2 48030639 1 COSM13395 MSH6 248030686 1 COSM1021299 MSH6 2 48030838 1 gDNA32 MSH6 2 209113112 1COSM28746 IDH1 2 209113119 1 COSM1404902 IDH1 2 209113140 1 COSM96922IDH1 2 212288955 1 COSM48362 ERBB4 2 212288964 1 COSM169572 ERBB4 2212530084 1 COSM232263 ERBB4 2 212530091 1 COSM573362 ERBB4 2 2125301351 COSM1405173 ERBB4 2 212576810 1 COSM1614287 ERBB4 2 212576877 1COSM110095 ERBB4 2 212576896 1 COSM573356 ERBB4 2 212578348 1COSM1405181 ERBB4 2 212578372 1 COSM160825 ERBB4 2 212587172 1COSM1015994 ERBB4 2 212587197 1 COSM1251447 ERBB4 2 212589812 1COSM1405184 ERBB4 2 212589838 1 COSM573353 ERBB4 2 212589909 1COSM1015997 ERBB4 Chromosome Position Mutation CDS 1 43814979c.1514G > A 1 43815009 c.1544G > T 1 43815020 c.1555G > A 1 115256529c.182A > G 1 115256537 c.174A > G 1 115256669 c.112 − 70C > T 1115258730 c.52G > A 1 115258747 c.35G > A 1 115258753 c.29G > A 229432664 c.3824G > A 2 29443695 c.3522C > A 2 48030632 c.3246G > T 248030639 c.3261delC 2 48030686 c.3300G > A 2 48030838 c.3438 + 14A > T 2209113112 c.395G > A 2 209113119 c.388A > G 2 209113140 c.367G > A 2212288955 c.2791G > T 2 212288964 c.2782G > T 2 212530084 c.1835G > A 2212530091 c.1828C > A 2 212530135 c.1784A > G 2 212576810 c.1089T > C 2212576877 c.1022C > T 2 212576896 c.1003G > T 2 212578348 c.909T > C 2212578372 c.885T > G 2 212587172 c.829C > A 2 212587197 c.804C > A 2212589812 c.730A > G 2 212589838 c.704C > T 2 212589909 c.633G > AMutation Target Sanger CHPv2 Chromosome Position Mutation AA Type StrandFrequency Detection* Detection 1 43814979 p.S505N SNV + 5-15% DetectedDetected 1 43815009 p.W515L SNV + 5-15% Detected Detected 1 43815020p.A519T SNV + 5-15% Detected Detected 1 115256529 p.Q61R SNV − 5-15%Detected Detected 1 115256537 p.T58T SNV − 5-15% Detected Detected 1115256669 p.(=) SNV − genomic Not Covered Not Covered 1 115258730 p.A18TSNV − 5-15% Detected Detected 1 115258747 p.G12D SNV − 5-15% DetectedDetected 1 115258753 p.G10E SNV − 5-15% Detected Detected 2 29432664p.R1275Q SNV − 5-15% Detected Detected 2 29443695 p.F1174L SNV − 5-15%Detected Detected 2 48030632 p.P1082P SNV + 5-15% Detected Not Covered 248030639 p.F1088fs*2 DEL + 5-15% Detected Not Covered 2 48030686p.T1100T SNV + 5-15% Detected Not Covered 2 48030838 p.(=) SNV + genomicNot Covered Not Covered 2 209113112 p.R132H SNV − 5-15% DetectedDetected 2 209113119 p.I130V SNV − 5-15% Detected Detected 2 209113140p.G123R SNV − 5-15% Detected Detected 2 212288955 p.D931Y SNV − 5-15%Detected Detected 2 212288964 p.E928* SNV − 5-15% Detected Detected 2212530084 p.R612Q SNV − 5-15% Detected Detected 2 212530091 p.P610T SNV− 5-15% Detected Detected 2 212530135 p.D595G SNV − 5-15% DetectedDetected 2 212576810 p.N363N SNV − 5-15% Detected Detected 2 212576877p.S341L SNV − 5-15% Detected Detected 2 212576896 p.D335Y SNV − 5-15%Detected Detected 2 212578348 p.S303S SNV − 5-15% Detected Detected 2212578372 p.H295Q SNV − 5-15% Detected Detected 2 212587172 p.H277N SNV− 5-15% Detected Detected 2 212587197 p.Y268* SNV − 5-15% DetectedDetected 2 212589812 p.T244A SNV − 5-15% Detected Detected 2 212589838p.A235V SNV − 5-15% Detected Detected 2 212589909 p.T211T SNV − 5-15%Detected Not Covered TSACP TSTP Chromosome Position Detection Detection1 43814979 Not Covered Not Covered 1 43815009 Detected Not Covered 143815020 Detected Not Covered 1 115256529 Detected Detected 1 115256537Detected Detected 1 115256669 Not Covered Detected 1 115258730 DetectedDetected 1 115258747 Detected Detected 1 115258753 Detected Detected 229432664 Detected Not Covered 2 29443695 Detected Detected 2 48030632Not Covered Detected 2 48030639 Not Covered Detected 2 48030686 NotCovered Detected 2 48030838 Not Covered Detected 2 209113112 DetectedNot Covered 2 209113119 Detected Not Covered 2 209113140 Detected NotCovered 2 212288955 Detected Not Covered 2 212288964 Detected NotCovered 2 212530084 Detected Not Covered 2 212530091 Detected NotCovered 2 212530135 Detected Not Covered 2 212576810 Not Covered NotCovered 2 212576877 Detected Not Covered 2 212576896 Detected NotCovered 2 212578348 Detected Not Covered 2 212578372 Detected NotCovered 2 212587172 Detected Not Covered 2 212587197 Detected NotCovered 2 212589812 Detected Not Covered 2 212589838 Detected NotCovered 2 212589909 Detected Not Covered Chromosome Position Reference 2212652764 T 2 212652791 G 3 10183797 T 3 10183808 G 3 10183817 C 310183824 AC 3 10188200 C 3 10188210 T 3 10188245 G 3 10188286 CG 310191479 C 3 10191488 C 3 10191506 C 3 10191513 T 3 37067240 T 341266101 C 3 41266113 C 3 41266124 A 3 41266137 C 3 138665163 G 3178916648 G 3 178916706 A 3 178916793 A 3 178916823 C 3 178916936 G 3178916944 A 3 178916957 G 3 178917661 A 3 178921489 C 3 178921520 C 3178921553 T 3 178927450 T 3 178927980 T Chromosome Position Alternate 2212652764 C 2 212652791 C 3 10183797 A 3 10183808 C 3 10183817 T 310183824 A 3 10188200 A 3 10188210 C 3 10188245 C 3 10188286 C 310191479 G 3 10191488 T 3 10191506 T 3 10191513 C 3 37067240 A 341266101 G 3 41266113 T 3 41266124 G 3 41266137 T 3 138665163 C 3178916648 A 3 178916706 G 3 178916793 G 3 178916823 T 3 178916936 A 3178916944 G 3 178916957 T 3 178917661 G 3 178921489 T 3 178921520 T 3178921553 A 3 178927450 C 3 178927980 C Chromosome Position LengthMutation ID Gene 2 212652764 1 COSM48369 ERBB4 2 212652791 1 COSM442267ERBB4 3 10183797 1 COSM14305 VHL 3 10183808 1 COSM18080 VHL 3 10183817 1COSM17658 VHL 3 10183824 1 COSM17886 VHL 3 10188200 1 COSM17752 VHL 310188210 1 COSM14312 VHL 3 10188245 1 COSM14407 VHL 3 10188286 1COSM14412 VHL 3 10191479 1 COSM17657 VHL 3 10191488 1 COSM17612 VHL 310191506 1 COSM14311 VHL 3 10191513 1 COSM17837 VHL 3 37067240 1COSM26085 MLH1 3 41266101 1 COSM5677 CTNNB1 3 41266113 1 COSM5662 CTNNB13 41266124 1 COSM5664 CTNNB1 3 41266137 1 COSM5667 CTNNB1 3 138665163 1COSM33661 FOXL2 3 178916648 1 COSM27495 PIK3CA 3 178916706 1 COSM27376PIK3CA 3 178916793 1 COSM1420738 PIK3CA 3 178916823 1 COSM1041454 PIK3CA3 178916936 1 COSM27497 PIK3CA 3 178916944 1 COSM13570 PIK3CA 3178916957 1 COSM125368 PIK3CA 3 178917661 1 COSM1420774 PIK3CA 3178921489 1 COSM21462 PIK3CA 3 178921520 1 COSM353193 PIK3CA 3 1789215531 COSM754 PIK3CA 3 178927450 1 COSM1420804 PIK3CA 3 178927980 1 COSM757PIK3CA Chromosome Position Mutation CDS 2 212652764 c.542A > G 2212652791 c.515C > G 3 10183797 c.266T > A 3 10183808 c.277G > C 310183817 c.286C > T 3 10183824 c.296delC 3 10188200 c.343C > A 310188210 c.353T > C 3 10188245 c.388G > C 3 10188286 c.431delG 310191479 c.472C > G 3 10191488 c.481C > T 3 10191506 c.499C > T 310191513 c.506T > C 3 37067240 c.1151T > A 3 41266101 c.98C > G 341266113 c.110C > T 3 41266124 c.121A > G 3 41266137 c.134C > T 3138665163 c.402C > G 3 178916648 c.35G > A 3 178916706 c.93A > G 3178916793 c.180A > G 3 178916823 c.210C > T 3 178916936 c.323G > A 3178916944 c.331A > G 3 178916957 c.344G > T 3 178917661 c.536A > G 3178921489 c.971C > T 3 178921520 c.1002C > T 3 178921553 c.1035T > A 3178927450 c.1213T > C 3 178927980 c.1258T > C Mutation Target SangerCHPv2 Chromosome Position Mutation AA Type Strand Frequency Detection*Detection 2 212652764 p.N181S SNV − 5-15% Detected Detected 2 212652791p.P172R SNV − 5-15% Detected Detected 3 10183797 p.L89H SNV + 5-15%Detected Detected 3 10183808 p.G93R SNV + 5-15% Detected Detected 310183817 p.Q96* SNV + 5-15% Detected Detected 3 10183824 p.P99fs*60DEL + 5-15% Detected Detected 3 10188200 p.H115N SNV + 5-15% DetectedDetected 3 10188210 p.L118P SNV + 5-15% Detected Detected 3 10188245p.V130L SNV + 5-15% Detected Detected 3 10188286 p.G144fs*15 DEL + 5-15%Detected Detected 3 10191479 p.L158V SNV + 5-15% Detected Detected 310191488 p.R161* SNV + 5-15% Detected Detected 3 10191506 p.R167W SNV +5-15% Detected Detected 3 10191513 p.L169P SNV + 5-15% Detected Detected3 37067240 p.V384D SNV + 5-15% Detected Detected 3 41266101 p.S33C SNV +5-15% Detected Detected 3 41266113 p.S37F SNV + 5-15% Detected Detected3 41266124 p.T41A SNV + 5-15% Detected Detected 3 41266137 p.S45F SNV +5-15% Detected Detected 3 138665163 p.C134W SNV − 5-15% Detected NotCovered 3 178916648 p.G12D SNV + 5-15% Detected Not Covered 3 178916706p.131M SNV + 5-15% Detected Not Covered 3 178916793 p.Q60Q SNV + 5-15%Detected Detected 3 178916823 p.F70F SNV + 5-15% Detected Detected 3178916936 p.R108H SNV + 5-15% Detected Detected 3 178916944 p.K111ESNV + 5-15% Detected Detected 3 178916957 p.R115L SNV + 5-15% DetectedDetected 3 178917661 p.K179R SNV + 5-15% Detected Not Covered 3178921489 p.T3241 SNV + 5-15% Detected Detected 3 178921520 p.L334LSNV + 5-15% Detected Detected 3 178921553 p.N345K SNV + 5-15% DetectedDetected 3 178927450 p.S405P SNV + 5-15% Detected Detected 3 178927980p.C420R SNV + 5-15% Detected Detected TSACP TSTP Chromosome PositionDetection Detection 2 212652764 Detected Not Covered 2 212652791Detected Not Covered 3 10183797 Detected Not Covered 3 10183808 DetectedNot Covered 3 10183817 Detected Not Covered 3 10183824 Detected NotCovered 3 10188200 Not Covered Not Covered 3 10188210 Not Covered NotCovered 3 10188245 Detected Not Covered 3 10188286 Detected Not Covered3 10191479 Not Detected Not Covered 3 10191488 Detected Not Covered 310191506 Detected Not Covered 3 10191513 Not Detected Not Covered 337067240 Detected Not Covered 3 41266101 Detected Detected 3 41266113Detected Detected 3 41266124 Detected Detected 3 41266137 DetectedDetected 3 138665163 Not Covered Detected 3 178916648 Not CoveredDetected 3 178916706 Not Covered Detected 3 178916793 Not CoveredDetected 3 178916823 Not Covered Detected 3 178916936 Detected Detected3 178916944 Detected Detected 3 178916957 Detected Detected 3 178917661Not Covered Detected 3 178921489 Not Covered Not Covered 3 178921520 NotCovered Not Covered 3 178921553 Detected Not Covered 3 178927450 NotCovered Not Covered 3 178927980 Detected Detected Chromosome PositionReference 3 178928092 A 3 178936074 C 3 178936082 G 3 178936091 G 3178936098 A 3 178938860 A 3 178947827 G 3 178947850 T 3 178952055 A 3178952085 A 3 178952149 C 4 1803568 C 4 1803575 C 4 1803668 GC 4 1806089G 4 1806119 G 4 1806131 T 4 1806153 C 4 1807869 A 4 1807889 A 4 1807894G 4 1808331 G 4 1808962 A 4 55141051 GCCCAGATGGACATGA (SEQ ID NO: 19) 455141055 A 4 55141097 T 4 55144148 C 4 55144172 A 4 55144547 C 455151958 T 4 55152085 G 4 55152093 A 4 55152112 C Chromosome PositionAlternate 3 178928092 G 3 178936074 G 3 178936082 A 3 178936091 A 3178936098 G 3 178938860 C 3 178947827 T 3 178947850 C 3 178952055 G 3178952085 G 3 178952149 CA 4 1803568 G 4 1803575 T 4 1803668 G 4 1806089T 4 1806119 A 4 1806131 C 4 1806153 A 4 1807869 G 4 1807889 G 4 1807894A 4 1808331 T 4 1808962 C 4 55141051 G 4 55141055 G 4 55141097 C 455144148 A 4 55144172 G 4 55144547 T 4 55151958 TA 4 55152085 T 455152093 T 4 55152112 A Chromosome Position Length Mutation ID Gene 3178928092 1 COSM1420828 PIK3CA 3 178936074 1 COSM759 PIK3CA 3 1789360821 COSM760 PIK3CA 3 178936091 1 COSM763 PIK3CA 3 178936098 1 COSM1420865PIK3CA 3 178938860 1 COSM778 PIK3CA 3 178947827 1 COSM769 PIK3CA 3178947850 1 COSM770 PIK3CA 3 178952055 1 COSM328026 PIK3CA 3 178952085 1COSM775 PIK3CA 3 178952149 1 COSM12464 PIK3CA 4 1803568 1 COSM715 FGFR34 1803575 1 COSM29446 FGFR3 4 1803668 1 COSM723 FGFR3 4 1806089 1COSM716 FGFR3 4 1806119 1 COSM24842 FGFR3 4 1806131 1 COSM724 FGFR3 41806153 1 COSM721 FGFR3 4 1807869 1 COSM1428724 FGFR3 4 1807889 1COSM719 FGFR3 4 1807894 1 gDNA1 FGFR3 4 1808331 1 COSM24802 FGFR3 41808962 1 AMXsyntl FGFR3 4 55141051 15 COSM12418 PDGFRA 4 55141055 1gDNA2, COSM1430082 PDGFRA 4 55141097 1 COSM1430085 PDGFRA 4 55144148 1COSM22415 PDGFRA 4 55144172 1 COSM1430086 PDGFRA 4 55144547 1 COSM743PDGFRA 4 55151958 1 gDNA33 PDGFRA 4 55152085 1 COSM587613 PDGFRA 455152093 1 COSM736 PDGFRA 4 55152112 1 COSM28052 PDGFRA ChromosomePosition Mutation CDS 3 178928092 c.1370A > G 3 178936074 c.1616C > G 3178936082 c.1624G > A 3 178936091 c.1633G > A 3 178936098 c.1640A > G 3178938860 c.2102A > C 3 178947827 c.2702G > T 3 178947850 c.2725T > C 3178952055 c.3110A > G 3 178952085 c.3140A > G 3 178952149c.3204_3205insA 4 1803568 c.746C > G 4 1803575 c.753C > T 4 1803668c.850delC 4 1806089 c.1108G > T 4 1806119 c.1138G > A 4 1806131c.1150T > C 4 1806153 c.1172C > A 4 1807869 c.1928A > G 4 1807889c.1948A > G 4 1807894 c.1959A > G 4 1808331 c.2089G > T 4 1808962c.2401A > C 4 55141051 c.1698_1712del15 4 55141055 c.1701A > G 455141097 c.1743T > C 4 55144148 c.1977C > A 4 55144172 c.2001A > G 455144547 c.2021C > T 4 55151958 c.2440 − 50 c.2440 − 49insA 4 55152085c.2517G > T 4 55152093 c.2525A > T 4 55152112 c.2544C > A MutationTarget Sanger Chromosome Position Mutation AA Type Strand FrequencyDetection* 3 178928092 p.N457S SNV + 5-15% Detected 3 178936074 p.P539RSNV + 5-15% Detected 3 178936082 p.E542K SNV + 5-15% Detected 3178936091 p.E545K SNV + 5-15% Detected 3 178936098 p.E547G SNV + 5-15%Detected 3 178938860 p.H701P SNV + 5-15% Detected 3 178947827 p.C901FSNV + 5-15% Detected 3 178947850 p.F909L SNV + 5-15% Detected 3178952055 p.E1037G SNV + 5-15% Detected 3 178952085 p.H1047R SNV + 5-15%Detected 3 178952149 p.N1068fs*4 INS + 5-15% Detected 4 1803568 p.S249CSNV + 5-15% Detected 4 1803575 p.H251H SNV + 5-15% Detected 4 1803668p.H284fs*10 DEL + 5-15% Detected 4 1806089 p.G370C SNV + 5-15% Detected4 1806119 p.G380R SNV + 5-15% Detected 4 1806131 p.F384L SNV + 5-15%Detected 4 1806153 p.A391E SNV + 5-15% Detected 4 1807869 p.H643R SNV +5-15% Detected 4 1807889 p.K650E SNV + 5-15% Detected 4 1807894 p.T651TSNV + genomic Not Covered 4 1808331 p.G697C SNV + 5-15% Detected 41808962 p.P800P SNV + 5-15% Detected 4 55141051 p.S566 E571 > R DEL +5-15% Detected 4 55141055 p.P567P SNV + genomic Not Covered 4 55141097p.P581P SNV + 5-15% Detected 4 55144148 p.N659K SNV + 5-15% Detected 455144172 p.S667S SNV + 5-15% Detected 4 55144547 p.T674I SNV + 5-15%Detected 4 55151958 p.(=) INS + genomic Not Covered 4 55152085 p.L839LSNV + 5-15% Detected 4 55152093 p.D842V SNV + 5-15% Detected 4 55152112p.N848K SNV + 5-15% Detected CHPv2 TSACP TSTP Chromosome PositionDetection Detection Detection 3 178928092 Detected Not Covered Detected3 178936074 Detected Detected Detected 3 178936082 Detected DetectedDetected 3 178936091 Detected Detected Detected 3 178936098 DetectedDetected Detected 3 178938860 Detected Detected Not Covered 3 178947827Detected Not Covered Not Covered 3 178947850 Detected Not Covered NotCovered 3 178952055 Detected Not Detected Detected 3 178952085 DetectedNot Detected Detected 3 178952149 Detected Detected Not Detected 41803568 Detected Detected Not Covered 4 1803575 Detected Detected NotCovered 4 1803668 Not Covered Detected Not Covered 4 1806089 DetectedNot Covered Not Covered 4 1806119 Detected Detected Not Covered 41806131 Detected Detected Not Covered 4 1806153 Detected Detected NotCovered 4 1807869 Detected Detected Not Covered 4 1807889 DetectedDetected Not Covered 4 1807894 Detected Detected Not Covered 4 1808331Detected Not Detected Not Covered 4 1808962 Detected Detected NotCovered 4 55141051 Detected Detected Detected 4 55141055 DetectedDetected Detected 4 55141097 Detected Detected Detected 4 55144148Detected Detected Detected 4 55144172 Detected Detected Detected 455144547 Detected Detected Not Covered 4 55151958 Not Covered NotCovered Detected 4 55152085 Detected Detected Detected 4 55152093Detected Detected Detected 4 55152112 Detected Detected DetectedChromosome Position Reference 4 55561702 C 4 55561764 G 4 55561828 A 455592081 T 4 55592092 A 4 55592178 C 4 55592192 T 4 55592202 A 455592211 A 4 55593431 G 4 55593464 A 4 55593632 C 4 55593661 T 455593689 C 4 55594221 A 4 55594258 T 4 55595599 C 4 55597500 T 455597561 G 4 55599284 C 4 55599401 T 4 55599436 T 4 55602737 G 455602765 G 4 55946081 A 4 55946171 G 4 55953816ACTTCCTCCTCCTCCATACAGGAAAC (SEQ ID NO: 20) 4 55955112 C 4 55961023 C 455962505 T 4 55962545 T 4 55972974 T 4 55972978CTATAAGAAAGAGATAACAGCGCATATTATGATTTAATTTTT (SEQ ID NO: 21) ChromosomePosition Alternate 4 55561702 T 4 55561764 A 4 55561828 G 4 55592081 C 455592092 G 4 55592178 CTGCCTA 4 55592192 C 4 55592202 T 4 55592211 G 455593431 A 4 55593464 C 4 55593632 T 4 55593661 C 4 55593689 T 455594221 G 4 55594258 C 4 55595599 T 4 55597500 C 4 55597561 A 455599284 T 4 55599401 A 4 55599436 C 4 55602737 A 4 55602765 C 455946081 G 4 55946171 A 4 55953816 A 4 55955112 T 4 55961023 A 455962505 C 4 55962545 TG 4 55972974 A 4 55972978 C Chromosome PositionLength Mutation ID Gene 4 55561702 1 COSM77973 KIT 4 55561764 1 COSM1146KIT 4 55561828 1 COSM1430106 KIT 4 55592081 1 COSM24637 KIT 4 55592092 1COSM41602 KIT 4 55592178 6 COSM1326 KIT 4 55592192 1 COSM96867 KIT 455592202 1 COSM96885 KIT 4 55592211 1 COSM1430136 KIT 4 55593431 1COSM1155 KIT 4 55593464 1 gDNA3, COSM28026 KIT 4 55593632 1 COSM1275 KIT4 55593661 1 COSM1290 KIT 4 55593689 1 COSM1299 KIT 4 55594221 1COSM1304 KIT 4 55594258 1 COSM12706 KIT 4 55595599 1 COSM36053 KIT 455597500 1 COSM1430171 KIT 4 55597561 1 COSM21303 KIT 4 55599284 1COSM20402 KIT 4 55599401 1 COSM19194 KIT 4 55599436 1 gDNA4 KIT 455602737 1 COSM133767 KIT 4 55602765 1 gDNA5, COSM1325 KIT 4 55946081 1gDNA6 KDR 4 55946171 1 COSM35855 KDR 4 55953816 25 AMXsynt2 KDR 455955112 1 COSM1430203 KDR 4 55961023 1 COSM48464 KDR 4 55962505 1COSM1430212 KDR 4 55962545 1 gDNA7 KDR 4 55972974 1 gDNA8, COSM149673KDR 4 55972978 41 AMXsynt3 KDR Chromosome Position Mutation CDS 455561702 c.92C > T 4 55561764 c.154G > A 4 55561828 c.218A > G 455592081 c.1405T > C 4 55592092 c.1416A > G 4 55592178c.1509_1510insGCCTAT 4 55592192 c.1516T > C 4 55592202 c.1526A > T 455592211 c.1535A > G 4 55593431 c.1588G > A 4 55593464 c.1621A > C 455593632 c.1698C > T 4 55593661 c.1727T > C 4 55593689 c.1755C > T 455594221 c.1924A > G 4 55594258 c.1961T > C 4 55595599 c.2089C > T 455597500 c.2148T > C 4 55597561 c.2209G > A 4 55599284 c.2410C > T 455599401 c.2484 + 43T > A 4 55599436 c.2484 + 78T > C 4 55602737c.2558G > A 4 55602765 c.2586G > C 4 55946081 c.*27T > C 4 55946171c.4008C > T 4 55953816 c.3594del25 4 55955112 c.3433G > A 4 55961023c.2917G > T 4 55962505 c.2619A > G 4 55962545 c.2615 − 37_2615 − 36insC4 55972974 c.1416A > T 4 55972978 c.1413 − 42del41 Mutation TargetSanger Chromosome Position Mutation AA Type Strand Frequency Detection*4 55561702 p.P31L SNV + 5-15% Detected 4 55561764 p.D52N SNV + 5-15%Detected 4 55561828 p.E73G SNV + 5-15% Detected 4 55592081 p.F469L SNV +5-15% Detected 4 55592092 p.L472L SNV + 5-15% Detected 4 55592178p.Y503_F504insAY INS + 5-15% Detected 4 55592192 p.F506L SNV + 5-15%Detected 4 55592202 p.K509I SNV + 5-15% Detected 4 55592211 p.N512SSNV + 5-15% Detected 4 55593431 p.V530I SNV + 5-15% Detected 4 55593464p.M541L SNV + genomic Not Covered 4 55593632 p.N566N SNV + 5-15%Detected 4 55593661 p.L576P SNV + 5-15% Detected 4 55593689 p.P585PSNV + 5-15% Detected 4 55594221 p.K642E SNV + 5-15% Detected 4 55594258p.V654A SNV + 5-15% Detected 4 55595599 p.H697Y SNV + 5-15% Detected 455597500 p.D716D SNV + 5-15% Detected 4 55597561 p.D737N SNV + 5-15%Detected 4 55599284 p.R804W SNV + 5-15% Detected 4 55599401 p.? SNV +5-15% Detected 4 55599436 p.(=) SNV + genomic Not Covered 4 55602737p.W853* SNV + 5-15% Detected 4 55602765 p.L862L SNV + genomic NotCovered 4 55946081 p.(=) SNV − genomic Not Covered 4 55946171 p.T1336TSNV − 5-15% Detected 4 55953816 p.V1199fs*27 DEL − 5-15% Detected 455955112 p.G1145R SNV − 5-15% Detected 4 55961023 p.A973S SNV − 5-15%Detected 4 55962505 p.G873G SNV − 5-15% Detected 4 55962545 p.(=) INS −genomic Not Covered 4 55972974 p.Q472H SNV − genomic Not Covered 455972978 p.? DEL − 5-15% Detected CHPv2 TSACP TSTP Chromosome PositionDetection Detection Detection 4 55561702 Detected Not Covered NotCovered 4 55561764 Detected Detected Not Covered 4 55561828 Not CoveredDetected Not Covered 4 55592081 Not Covered Not Covered Detected 455592092 Not Covered Not Covered Detected 4 55592178 Detected NotCovered Detected 4 55592192 Detected Detected Detected 4 55592202Detected Detected Detected 4 55592211 Detected Detected Detected 455593431 Detected Detected Not Covered 4 55593464 Detected Detected NotCovered 4 55593632 Detected Detected Detected 4 55593661 DetectedDetected Detected 4 55593689 Detected Detected Detected 4 55594221Detected Detected Detected 4 55594258 Detected Detected Detected 455595599 Not Covered Detected Not Covered 4 55597500 Detected DetectedNot Covered 4 55597561 Not Covered Detected Not Covered 4 55599284Detected Not Covered Detected 4 55599401 Not Covered Detected Detected 455599436 Not Covered Detected Not Detected 4 55602737 Detected DetectedDetected 4 55602765 Not Covered Detected Detected 4 55946081 Not CoveredDetected Not Covered 4 55946171 Detected Detected Not Covered 4 55953816Detected Detected Not Covered 4 55955112 Detected Detected Not Covered 455961023 Detected Detected Not Covered 4 55962505 Detected Detected NotCovered 4 55962545 Detected Detected Not Covered 4 55972974 DetectedDetected Not Covered 4 55972978 Detected Not Detected Not CoveredChromosome Position Reference 4 55979623 C 4 55980239 C 4 153244078 T 4153244092 G 4 153244124 G 4 153244155 TC 4 153245477 T 4 153247222 T 4153247226 A 4 153247244 C 4 153247351 C 4 153247366 C 4 153249384 C 4153249440 C 4 153249456 C 4 153250883 G 4 153258983 G 4 153259071 C 5112173830 G 5 112173917 C 5 112173930 T 5 112173947 C 5 112174043 G 5112174577 C 5 112174596 A 5 112174726 A 5 112174989 CA 5 112175086 A 5112175162 C 5 112175171 C 5 112175211 T 5 112175255 G 5 112175348 GChromosome Position Alternate 4 55979623 A 4 55980239 T 4 153244078 C 4153244092 A 4 153244124 C 4 153244155 T 4 153245477TGATCATATTCATATTCTCTGAAATCAACGAG (SEQ ID NO: 22) 4 153247222 C 4153247226 G 4 153247244 T 4 153247351 A 4 153247366 T 4 153249384 T 4153249440 T 4 153249456 A 4 153250883 A 4 153258983 A 4 153259071 A 5112173830 GA 5 112173917 T 5 112173930 C 5 112173947 T 5 112174043 T 5112174577 T 5 112174596 G 5 112174726 G 5 112174989 C 5 112175086 G 5112175162 T 5 112175171 T 5 112175211 TA 5 112175255 T 5 112175348 TChromosome Position Length Mutation ID Gene 4 55979623 1 COSM32339 KDR 455980239 1 gDNA9 KDR 4 153244078 1 COSM1427592 FBXW7 4 153244092 1COSM27083 FBXW7 4 153244124 1 COSM732399 FBXW7 4 153244155 1 COSM34018FBXW7 4 153245477 31 AMXsynt4 FBXW7 4 153247222 1 COSM27913 FBXW7 4153247226 1 COSM30599 FBXW7 4 153247244 1 COSM30598 FBXW7 4 153247351 1COSM34016 FBXW7 4 153247366 1 COSM22974 FBXW7 4 153249384 1 COSM22965FBXW7 4 153249440 1 COSM22986 FBXW7 4 153249456 1 COSM161024 FBXW7 4153250883 1 COSM22973 FBXW7 4 153258983 1 COSM22971 FBXW7 4 153259071 1COSM1052125 FBXW7 5 112173830 1 COSM18979 APC 5 112173917 1 COSM18852APC 5 112173930 1 COSM19230 APC 5 112173947 1 COSM19330 APC 5 1121740431 COSM19065 APC 5 112174577 1 COSM13872 APC 5 112174596 1 COSM1432250APC 5 112174726 1 COSM1432260 APC 5 112174989 1 COSM41617 APC 5112175086 1 COSM1432280 APC 5 112175162 1 COSM19072 APC 5 112175171 1COSM18960 APC 5 112175211 1 COSM18719 APC 5 112175255 1 COSM18702 APC 5112175348 1 COSM19048 APC Chromosome Position Mutation CDS 4 55979623c.824G > T 4 55980239 c.798 + 54G > A 4 153244078 c.2079A > G 4153244092 c.2065C > T 4 153244124 c.2033C > G 4 153244155 c.2001delG 4153245477 c.1473_1474insCTCGTTGATTTCAGAGAATATGAATATGATC (SEQ ID NO: 23)4 153247222 c.1580A > G 4 153247226 c.1576T > C 4 153247244 c.1558G > A4 153247351 c.1451G > T 4 153247366 c.1436G > A 4 153249384 c.1394G > A4 153249440 c.1338G > A 4 153249456 c.1322G > T 4 153250883 c.1177C > T4 153258983 c.832C > T 4 153259071 c.744G > T 5 112173830c.2543_2544insA 5 112173917 c.2626C > T 5 112173930 c.2639T > C 5112173947 c.2656C > T 5 112174043 c.2752G > T 5 112174577 c.3286C > T 5112174596 c.3305A > G 5 112174726 c.3435A > G 5 112174989 c.3700delA 5112175086 c.3795A > G 5 112175162 c.3871C > T 5 112175171 c.3880C > T 5112175211 c.3923_3924insA 5 112175255 c.3964G > T 5 112175348c.4057G > T Mutation Target Sanger Chromosome Position Mutation AA TypeStrand Frequency Detection* 4 55979623 p.R275L SNV − 5-15% Detected 455980239 p.(=) SNV − genomic Not Covered 4 153244078 p.E693E SNV − 5-15%Detected 4 153244092 p.R689W SNV − 5-15% Detected 4 153244124 p.S678*SNV − 5-15% Detected 4 153244155 p.S668fs*39 DEL − 5-15% Detected 4153245477 p.N492fs*42 INS − 5-15% Detected 4 153247222 p.D527G SNV −5-15% Detected 4 153247226 p.W526R SNV − 5-15% Detected 4 153247244p.D520N SNV − 5-15% Detected 4 153247351 p.R484M SNV − 5-15% Detected 4153247366 p.R479Q SNV − 5-15% Detected 4 153249384 p.R465H SNV − 5-15%Detected 4 153249440 p.W446* SNV − 5-15% Detected 4 153249456 p.R441LSNV − 5-15% Detected 4 153250883 p.R393* SNV − 5-15% Detected 4153258983 p.R278* SNV − 5-15% Detected 4 153259071 p.E248D SNV − 5-15%Detected 5 112173830 p.D849fs*2 INS + 15-35%  Detected 5 112173917p.R876* SNV + 15-35%  Detected 5 112173930 p.1880T SNV + 15-35% Detected 5 112173947 p.Q886* SNV + 15-35%  Detected 5 112174043 p.E918*SNV + 15-35%  Detected 5 112174577 p.Q1096* SNV + 15-35%  Detected 5112174596 p.Y1102C SNV + 15-35%  Detected 5 112174726 p.E1145E SNV +15-35%  Detected 5 112174989 p.S1234fs*31 DEL + 15-35%  Detected 5112175086 p.E1265E SNV + 15-35%  Detected 5 112175162 p.Q1291* SNV +15-35%  Detected 5 112175171 p.Q1294* SNV + 15-35%  Detected 5 112175211p.E1309fs*6 INS + 15-35%  Detected 5 112175255 p.E1322* SNV + 15-35%Detected 5 112175348 p.E1353* SNV + 15-35% Detected CHPv2 TSACP TSTPChromosome Position Detection Detection Detection 4 55979623 DetectedDetected Not Covered 4 55980239 Detected Not Covered Not Covered 4153244078 Not Covered Not Covered Detected 4 153244092 Not Covered NotCovered Detected 4 153244124 Not Covered Not Covered Detected 4153244155 Not Covered Not Covered Detected 4 153245477 Not DetectedDetected Detected 4 153247222 Not Covered Not Covered Detected 4153247226 Not Covered Not Covered Detected 4 153247244 Not Covered NotCovered Detected 4 153247351 Detected Detected Detected 4 153247366Detected Detected Detected 4 153249384 Detected Detected Detected 4153249440 Detected Detected Detected 4 153249456 Detected DetectedDetected 4 153250883 Detected Detected Detected 4 153258983 DetectedDetected Not Covered 4 153259071 Not Covered Detected Not Covered 5112173830 Not Covered Not Covered Detected 5 112173917 Detected DetectedDetected 5 112173930 Detected Detected Detected 5 112173947 DetectedDetected Detected 5 112174043 Not Covered Detected Not Covered 5112174577 Detected Not Covered Detected 5 112174596 Detected Not CoveredDetected 5 112174726 Not Covered Detected Detected 5 112174989 NotCovered Not Covered Detected 5 112175086 Not Covered Detected Detected 5112175162 Detected Detected Detected 5 112175171 Detected DetectedDetected 5 112175211 Detected Detected Detected 5 112175255 DetectedDetected Detected 5 112175348 Detected Detected Detected ChromosomePosition Reference 5 112175354 T 5 112175423 C 5 112175432 C 5 112175479TGA 5 112175507 C 5 112175576 C 5 112175675 AAG 5 112175830 GC 5112175852 G 5 112175930 G 5 112175945 G 5 112175951 G 5 112176063 C 5112176117 C 5 149433596 T 5 149433597 G 5 149433645 T 5 149433673 C 5149453057 C 5 170837543 C 7 55211080 G 7 55211097 G 7 55211165 C 755221822 C 7 55221830 G 7 55233043 G 7 55233109 G 7 55241615 T 755241644 G 7 55241708 G 7 55241722 G 7 55241755 G 7 55242427 CChromosome Position Alternate 5 112175354 C 5 112175423 T 5 112175432 T5 112175479 T 5 112175507 T 5 112175576 T 5 112175675 A 5 112175830 G 5112175852 T 5 112175930 T 5 112175945 T 5 112175951 GA 5 112176063 CA 5112176117 T 5 149433596 G 5 149433597 A 5 149433645 C 5 149433673 T 5149453057 CACTGCTTGA (SEQ ID NO: 24) 5 170837543 CTCTG 7 55211080 A 755211097 A 7 55211165 T 7 55221822 T 7 55221830 T 7 55233043 T 755233109 A 7 55241615 C 7 55241644 A 7 55241708 C 7 55241722 A 755241755 A 7 55242427 T Chromosome Position Length Mutation ID Gene 5112175354 1 COSM19652 APC 5 112175423 1 COSM18862 APC 5 112175432 1COSM143913 APC 5 112175479 2 COSM18993 APC 5 112175507 1 COSM19087 APC 5112175576 1 COSM18836 APC 5 112175675 2 COSM13864 APC 5 112175830 1COSM1173082 APC 5 112175852 1 COSM1183180 APC 5 112175930 1 COSM13879APC 5 112175945 1 COSM41616 APC 5 112175951 1 COSM18561 APC 5 1121760631 COSM18875 APC 5 112176117 1 COSM42906 APC 5 149433596 1 gDNA10 CSF1R 5149433597 1 gDNAll CSF1R 5 149433645 1 COSM947 CSF1R 5 149433673 1COSM310349 CSF1R 5 149453057 9 AMXsynt5 CSF1R 5 170837543 4 COSM17559NPM1 7 55211080 1 COSM21683 EGFR 7 55211097 1 COSM174732 EGFR 7 552111651 COSM1451540 EGFR 7 55221822 1 COSM21687 EGFR 7 55221830 1 COSM43067EGFR 7 55233043 1 COSM21690 EGFR 7 55233109 1 COSM35825 EGFR 7 552416151 COSM13177 EGFR 7 55241644 1 COSM41905 EGFR 7 55241708 1 COSM6239 EGFR7 55241722 1 COSM13979 EGFR 7 55241755 1 gDNA15 EGFR 7 55242427 1COSM53194 EGFR Chromosome Position Mutation CDS 5 112175354 c.4063T > C5 112175423 c.4132C > T 5 112175432 c.4141C > T 5 112175479c.4189_4190delGA 5 112175507 c.4216C > T 5 112175576 c.4285C > T 5112175675 c.4393_4394delAG 5 112175830 c.4540delC 5 112175852c.4561G > T 5 112175930 c.4639G > T 5 112175945 c.4654G > T 5 112175951c.4666_4667insA 5 112176063 c.4773_4774insA 5 112176117 c.4826C > T 5149433596 c.*36A > C 5 149433597 c.*35C > T 5 149433645 c.2906A > G 5149433673 c.2878G > A 5 149453057 c.890 − 2_c.890 − 1insTCAAGCAGT 5170837543 c.863_864insTCTG 7 55211080 c.323G > A 7 55211097 c.340G > A 755211165 c.408C > T 7 55221822 c.866C > T 7 55221830 c.874G > T 755233043 c.1793G > T 7 55233109 c.1859G > A 7 55241615 c.2063T > C 755241644 c.2092G > A 7 55241708 c.2156G > C 7 55241722 c.2170G > A 755241755 c.2184 + 19G > A 7 55242427 c.2197C > T Mutation Target SangerChromosome Position Mutation AA Type Strand Frequency Detection* 5112175354 p.S1355P SNV + 15-35% Detected 5 112175423 p.Q1378* SNV +15-35% Detected 5 112175432 p.P1381S SNV + 15-35% Detected 5 112175479p.R1399fs*9 DEL + 15-35% Detected 5 112175507 p.Q1406* SNV + 15-35%Detected 5 112175576 p.Q1429* SNV + 15-35% Detected 5 112175675p.S1465fs*3 DEL + 15-35% Detected 5 112175830 p.P1514fs*9 DEL + 15-35%Detected 5 112175852 p.E1521* SNV + 15-35% Detected 5 112175930 p.E1547*SNV + 15-35% Detected 5 112175945 p.E1552* SNV + 15-35% Detected 5112175951 p.T1556fs*3 INS + 15-35% Detected 5 112176063 p.P1594fs*38INS + 15-35% Detected 5 112176117 p.P1609L SNV + 15-35% Detected 5149433596 p.(=) SNV − genomic Not Covered 5 149433597 p.(=) SNV −genomic Not Covered 5 149433645 p.Y969C SNV − 15-35% Detected 5149433673 p.A960T SNV − 15-35% Detected 5 149453057 p.? INS − 15-35%Detected 5 170837543 p.W288fs*12 INS + 15-35% Detected 7 55211080p.R108K SNV + 15-35% Detected 7 55211097 p.E114K SNV + 15-35% Detected 755211165 p.P136P SNV + 15-35% Detected 7 55221822 p.A289V SNV + 15-35%Detected 7 55221830 p.V292L SNV + 15-35% Detected 7 55233043 p.G598VSNV + 15-35% Detected 7 55233109 p.C620Y SNV + 15-35% Detected 755241615 p.L688P SNV + 15-35% Detected 7 55241644 p.A698T SNV + 15-35%Detected 7 55241708 p.G719A SNV + 15-35% Detected 7 55241722 p.G724SSNV + 15-35% Detected 7 55241755 p.(=) SNV + genomic Not Covered 755242427 p.P733S SNV + 15-35% Detected CHPv2 TSACP TSTP ChromosomePosition Detection Detection Detection 5 112175354 Detected DetectedDetected 5 112175423 Detected Detected Detected 5 112175432 DetectedDetected Detected 5 112175479 Not Covered Detected Detected 5 112175507Not Covered Detected Detected 5 112175576 Detected Detected Detected 5112175675 Detected Detected Detected 5 112175830 Detected DetectedDetected 5 112175852 Detected Detected Detected 5 112175930 DetectedDetected Detected 5 112175945 Detected Detected Detected 5 112175951Detected Detected Detected 5 112176063 Not Covered Not Covered Detected5 112176117 Not Covered Not Covered Detected 5 149433596 Detected NotCovered Not Covered 5 149433597 Detected Detected Not Covered 5149433645 Detected Detected Not Covered 5 149433673 Detected DetectedNot Covered 5 149453057 Detected Detected Not Covered 5 170837543Detected Detected Not Covered 7 55211080 Detected Detected Not Covered 755211097 Detected Detected Not Covered 7 55211165 Not Covered DetectedNot Covered 7 55221822 Detected Detected Not Covered 7 55221830 DetectedDetected Not Covered 7 55233043 Detected Detected Not Covered 7 55233109Not Covered Detected Not Covered 7 55241615 Not Covered Not CoveredDetected 7 55241644 Detected Not Covered Detected 7 55241708 DetectedDetected Detected 7 55241722 Detected Detected Detected 7 55241755 NotCovered Detected Not Detected 7 55242427 Detected Detected DetectedChromosome Position Reference 7 55242433 G 7 55242452 C 7 55242464AGGAATTAAGAGAAGC (SEQ ID NO: 25) 7 55248995 G 7 55249063 G 7 55249077 T7 55249131 G 7 55249143 T 7 55259427 G 7 55259439 T 7 55259446 A 755259457 G 7 55259515 T 7 55259524 T 7 55259530 G 7 55259554 C 7116339642 G 7 116340262 A 7 116412044 G 7 116417465 T 7 116417499 C 7116418969 G 7 116418997 C 7 116419008 T 7 116422133 T 7 116423428 T 7116423449 G 7 116423456 A 7 116423474 T 7 116436022 G 7 116436097 G 7128845101 C 7 128846040 G Chromosome Position Alternate 7 55242433 A 755242452 T 7 55242464 A 7 55248995 A 7 55249063 A 7 55249077 C 755249131 A 7 55249143 C 7 55259427 A 7 55259439 G 7 55259446 T 755259457 A 7 55259515 G 7 55259524 A 7 55259530 A 7 55259554 G 7116339642 T 7 116340262 G 7 116412044 A 7 116417465 C 7 116417499 G 7116418969 C 7 116418997 T 7 116419008 C 7 116422133 G 7 116423428 G 7116423449 T 7 116423456 G 7 116423474 C 7 116436022 A 7 116436097 A 7128845101 T 7 128846040 A Chromosome Position Length Mutation ID Gene 755242433 1 COSM13182 EGFR 7 55242452 1 COSM17570 EGFR 7 55242464 15COSM6223 EGFR 7 55248995 1 COSM28603 EGFR 7 55249063 1 gDNA16,COSM1451600 EGFR 7 55249077 1 COSM13190 EGFR 7 55249131 1 COSM12986 EGFR7 55249143 1 COSM28610 EGFR 7 55259427 1 COSM53291 EGFR 7 55259439 1COSM13424 EGFR 7 55259446 1 COSM6227 EGFR 7 55259457 1 COSM13430 EGFR 755259515 1 COSM6224 EGFR 7 55259524 1 COSM6213 EGFR 7 55259530 1COSM14070 EGFR 7 55259554 1 COSM13008 EGFR 7 116339642 1 COSM706 MET 7116340262 1 COSM710 MET 7 116412044 1 COSM29633 MET 7 116417465 1COSM1447462 MET 7 116417499 1 COSM697 MET 7 116418969 1 COSM43064 MET 7116418997 1 COSM1214928 MET 7 116419008 1 COSM1447471 MET 7 116422133 1COSM1330154 MET 7 116423428 1 COSM700 MET 7 116423449 1 COSM48565 MET 7116423456 1 COSM695 MET 7 116423474 1 COSM691 MET 7 116436022 1 gDNA12,COSM150378 MET 7 116436097 1 gDNA13, COSM150379 MET 7 128845101 1COSM13145 SMO 7 128846040 1 COSM13147 SMO Chromosome Position MutationCDS 7 55242433 c.2203G > A 7 55242452 c.2222C > T 7 55242464c.2235_2249del15 7 55248995 c.2293G > A 7 55249063 c.2361G > A 755249077 c.2375T > C 7 55249131 c.2429G > A 7 55249143 c.2441T > C 755259427 c.2485G > A 7 55259439 c.2497T > G 7 55259446 c.2504A > T 755259457 c.2515G > A 7 55259515 c.2573T > G 7 55259524 c.2582T > A 755259530 c.2588G > A 7 55259554 c.2612C > G 7 116339642 c.504G > T 7116340262 c.1124A > G 7 116412044 c.3082 + 1G > A 7 116417465c.3336T > C 7 116417499 c.3370C > G 7 116418969 c.3534G > C 7 116418997c.3562C > T 7 116419008 c.3573T > C 7 116422133 c.3668T > G 7 116423428c.3757T > G 7 116423449 c.3778G > T 7 116423456 c.3785A > G 7 116423474c.3803T > C 7 116436022 c.4071G > A 7 116436097 c.4146G > A 7 128845101c.595C > T 7 128846040 c.970G > A Mutation Target Sanger ChromosomePosition Mutation AA Type Strand Frequency Detection* 7 55242433 p.G735SSNV + 15-35% Detected 7 55242452 p.P741L SNV + 15-35% Detected 755242464 p.E746_A750delELREA DEL + 15-35% Detected 7 55248995 p.V765MSNV + 15-35% Detected 7 55249063 p.Q787Q SNV + genomic Not Covered 755249077 p.L792P SNV + 15-35% Detected 7 55249131 p.G810D SNV + 15-35%Detected 7 55249143 p.L814P SNV + 15-35% Detected 7 55259427 p.E829KSNV + 15-35% Detected 7 55259439 p.L833V SNV + 15-35% Detected 755259446 p.H835L SNV + 15-35% Detected 7 55259457 p.A839T SNV + 15-35%Detected 7 55259515 p.L858R SNV + 15-35% Detected 7 55259524 p.L861QSNV + 15-35% Detected 7 55259530 p.G863D SNV + 15-35% Detected 755259554 p.A871G SNV + 15-35% Detected 7 116339642 p.E168D SNV + 15-35%Detected 7 116340262 p.N375S SNV + 15-35% Detected 7 116412044 p.? SNV +15-35% Detected 7 116417465 p.H1112H SNV + 15-35% Detected 7 116417499p.H1124D SNV + 15-35% Detected 7 116418969 p.M11781 SNV + 15-35%Detected 7 116418997 p.R1188* SNV + 15-35% Detected 7 116419008 p.T1191TSNV + 15-35% Detected 7 116422133 p.L1223W SNV + 15-35% Detected 7116423428 p.Y1253D SNV + 15-35% Detected 7 116423449 p.G1260C SNV +15-35% Detected 7 116423456 p.K1262R SNV + 15-35% Detected 7 116423474p.M1268T SNV + 15-35% Detected 7 116436022 p.A1357A SNV + genomic NotCovered 7 116436097 p.P1382P SNV + genomic Not Covered 7 128845101p.R199W SNV + 15-35% Detected 7 128846040 p.A324T SNV + 15-35% DetectedCHPv2 TSACP TSTP Chromosome Position Detection Detection Detection 755242433 Detected Detected Detected 7 55242452 Detected DetectedDetected 7 55242464 Detected Detected Detected 7 55248995 DetectedDetected Detected 7 55249063 Detected Detected Detected 7 55249077Detected Detected Detected 7 55249131 Detected Detected Detected 755249143 Detected Detected Detected 7 55259427 Not Covered Not CoveredDetected 7 55259439 Not Covered Not Covered Detected 7 55259446 NotCovered Not Covered Detected 7 55259457 Not Covered Not Covered Detected7 55259515 Detected Detected Detected 7 55259524 Detected DetectedDetected 7 55259530 Detected Detected Detected 7 55259554 DetectedDetected Detected 7 116339642 Detected Detected Detected 7 116340262Detected Detected Detected 7 116412044 Not Covered Detected Detected 7116417465 Detected Detected Detected 7 116417499 Detected DetectedDetected 7 116418969 Not Covered Not Covered Detected 7 116418997 NotCovered Not Covered Detected 7 116419008 Not Covered Not CoveredDetected 7 116422133 Not Covered Not Covered Detected 7 116423428Detected Detected Detected 7 116423449 Detected Detected Detected 7116423456 Detected Detected Detected 7 116423474 Detected DetectedDetected 7 116436022 Not Covered Not Covered Detected 7 116436097 NotCovered Not Covered Detected 7 128845101 Detected Detected Not Covered 7128846040 Detected Detected Not Covered Chromosome Position Reference 7128846398 C 7 128846469 A 7 128850341 G 7 128851593 A 7 140453136 A 7140453145 A 7 140453154 T 7 140453193 T 7 140481417 C 7 140481428 T 7140481449 A 7 140481478 G 7 148508727 T 8 38282147 G 8 38285864 G 838285891 T 8 38285938 G 9 5073770 G 9 5073781 C 9 21971000 C 9 21971017G 9 21971028 C 9 21971036 C 9 21971111 G 9 21971120 G 9 21971153 C 921971186 G 9 80336317 G 9 80343489 T 9 80343605 GAAAAAACAAGGA (SEQ IDNO: 26) 9 80409345 A 9 80409432 ACA 9 80409533TAATAACATATAAAGTAAAACTAAAAAGTCAACATAAATATA (SEQ ID NO: 27) ChromosomePosition Alternate 7 128846398 T 7 128846469 G 7 128850341 T 7 128851593G 7 140453136 T 7 140453145 C 7 140453154 C 7 140453193 C 7 140481417 A7 140481428 C 7 140481449 G 7 140481478 A 7 148508727 A 8 38282147 A 838285864 A 8 38285891 C 8 38285938 A 9 5073770 T 9 5073781 A 9 21971000A 9 21971017 A 9 21971028 T 9 21971036 A 9 21971111 A 9 21971120 A 921971153 A 9 21971186 A 9 80336317 A 9 80343489 TGTAC 9 80343605 G 980409345 G 9 80409432 TGC 9 80409533 T Chromosome Position LengthMutation ID Gene 7 128846398 1 COSM216037 SMO 7 128846469 1 gDNA14 SMO 7128850341 1 COSM13146 SMO 7 128851593 1 COSM13150 SMO 7 140453136 1COSM476 BRAF 7 140453145 1 COSM471 BRAF 7 140453154 1 COSM467 BRAF 7140453193 1 COSM462 BRAF 7 140481417 1 COSM450 BRAF 7 140481428 1COSM27986 BRAF 7 140481449 1 COSM1448625 BRAF 7 140481478 1 COSM6262BRAF 7 148508727 1 COSM37028 EZH2 8 38282147 1 COSM1292693 FGFR1 838285864 1 COSM187237 FGFR1 8 38285891 1 COSM1456955 FGFR1 8 38285938 1COSM601 FGFR1 9 5073770 1 COSM12600 JAK2 9 5073781 1 COSM27063 JAK2 921971000 1 COSM12479 CDKN2A 9 21971017 1 COSM12476 CDKN2A 9 21971028 1COSM12547 CDKN2A 9 21971036 1 COSM13489 CDKN2A 9 21971111 1 COSM12504CDKN2A 9 21971120 1 COSM12475 CDKN2A 9 21971153 1 COSM13281 CDKN2A 921971186 1 COSM12473 CDKN2A 9 80336317 1 COSM1110323 GNAQ 9 80343489 4AMXsynt6 GNAQ 9 80343605 12 AMXsynt7 GNAQ 9 80409345 1 gDNA17 GNAQ 980409432 3 AMXsynt8 GNAQ 9 80409533 41 AMXsynt9 GNAQ Chromosome PositionMutation CDS 7 128846398 c.1234C > T 7 128846469 c.1264 + 41A > G 7128850341 c.1604G > T 7 128851593 c.1918A > G 7 140453136 c.1799T > A 7140453145 c.1790T > G 7 140453154 c.1781A > G 7 140453193 c.1742A > G 7140481417 c.1391G > T 7 140481428 c.1380A > G 7 140481449 c.1359T > C 7140481478 c.1330C > T 7 148508727 c.1937A > T 8 38282147 c.816C > T 838285864 c.448C > T 8 38285891 c.421A > G 8 38285938 c.374C > T 95073770 c.1849G > T 9 5073781 c.1860C > A 9 21971000 c.358G > T 921971017 c.341C > T 9 21971028 c.330G > A 9 21971036 c.322G > T 921971111 c.247C > T 9 21971120 c.238C > T 9 21971153 c.205G > T 921971186 c.172C > T 9 80336317 c.1002C > T 9 80343489 c.829_830insGTAC 980343605 c.736 − 34del12 9 80409345 c.735 + 34T > C 9 80409432c.679_681TGT > GCA 9 80409533 c.606 − 66del41 Chromosome PositionMutation AA Mutation Type Strand Target Frequency 7 128846398 p.L412FSNV + 15-35% 7 128846469 p.(=) SNV + genomic 7 128850341 p.W535L SNV +15-35% 7 128851593 p.T640A SNV + 15-35% 7 140453136 p.V600E SNV − 15-35%7 140453145 p.L597R SNV − 15-35% 7 140453154 p.D594G SNV − 15-35% 7140453193 p.N581S SNV − 15-35% 7 140481417 p.G464V SNV − 15-35% 7140481428 p.G460G SNV − 15-35% 7 140481449 p.P453P SNV − 15-35% 7140481478 p.R444W SNV − 15-35% 7 148508727 p.Y646F SNV − 15-35% 838282147 p.N272N SNV − 15-35% 8 38285864 p.P150S SNV − 15-35% 8 38285891p.T141A SNV − 15-35% 8 38285938 p.S125L SNV − 15-35% 9 5073770 p.V617FSNV + 15-35% 9 5073781 p.D620E SNV + 15-35% 9 21971000 p.E120* SNV −15-35% 9 21971017 p.P114L SNV − 15-35% 9 21971028 p.W110* SNV − 15-35% 921971036 p.D108Y SNV − 15-35% 9 21971111 p.H83Y SNV − 15-35% 9 21971120p.R80* SNV − 15-35% 9 21971153 p.E69* SNV − 15-35% 9 21971186 p.R58* SNV− 15-35% 9 80336317 p.T334T SNV − 15-35% 9 80343489 p.D277fs*20 INS −15-35% 9 80343605 p.? DEL − 15-35% 9 80409345 p.(=) SNV − genomic 980409432 p.M227_F228 > SI MNV − 15-35% 9 80409533 p.? DEL − 15-35%Sanger CHPv2 TSACP TSTP Chromosome Position Detection* DetectionDetection Detection 7 128846398 Detected Detected Detected Not Covered 7128846469 Not Covered Not Covered Detected Not Covered 7 128850341Detected Detected Detected Not Covered 7 128851593 Detected DetectedDetected Not Covered 7 140453136 Detected Detected Detected Detected 7140453145 Detected Detected Detected Detected 7 140453154 DetectedDetected Detected Detected 7 140453193 Detected Detected DetectedDetected 7 140481417 Detected Detected Detected Detected 7 140481428Detected Detected Detected Detected 7 140481449 Detected DetectedDetected Detected 7 140481478 Detected Detected Detected Detected 7148508727 Detected Detected Not Covered Not Covered 8 38282147 DetectedDetected Not Covered Not Covered 8 38285864 Detected Detected NotCovered Not Covered 8 38285891 Detected Detected Not Covered Not Covered8 38285938 Detected Detected Detected Not Covered 9 5073770 DetectedDetected Detected Not Covered 9 5073781 Detected Detected Detected NotCovered 9 21971000 Detected Detected Not Covered Not Covered 9 21971017Detected Detected Not Covered Not Covered 9 21971028 Detected DetectedNot Covered Not Covered 9 21971036 Detected Detected Not Covered NotCovered 9 21971111 Detected Detected Not Covered Not Covered 9 21971120Detected Detected Not Covered Not Covered 9 21971153 Detected DetectedNot Detected Not Covered 9 21971186 Detected Detected Detected NotCovered 9 80336317 Detected Not Covered Detected Not Covered 9 80343489Detected Not Covered Detected Detected 9 80343605 Detected Not CoveredDetected Not Detected 9 80409345 Not Covered Not Covered Detected NotCovered 9 80409432 Detected Detected Detected Detected 9 80409533Detected Not Covered Not Detected Not Detected Chromosome PositionReference 9 80412493 C 9 80412518 T 9 133738342 C 9 133738349 G 9133738357 T 9 133738363 G 9 133747520 A 9 133747571 T 9 133748391 T 9133748403 A 9 133748414 T 9 133750319 C 9 133750356 A 9 139390779 G 9139390804 CG 9 139390816 G 9 139390873 G 9 139397768 A 9 139397776 G 9139399344 A 9 139399350 C 9 139399365 A 9 139399422 A 10  43609096 T 10 43609102 T 10  43609942 GAGCTGTGCCGCA (SEQ ID NO: 28) 10  43609990 G 10 43610039 C 10  43613840 G 10  43613843 G 10  43615568 GC 10  43615622 G10  43617416 T Chromosome Position Alternate 9 80412493 T 9 80412518 A 9133738342 G 9 133738349 A 9 133738357 C 9 133738363 A 9 133747520 G 9133747571 TGCC 9 133748391 C 9 133748403 G 9 133748414 G 9 133750319 A 9133750356 G 9 139390779 T 9 139390804 C 9 139390816 A 9 139390873 A 9139397768 G 9 139397776 A 9 139399344 G 9 139399350 G 9 139399365 G 9139399422 G 10  43609096 C 10  43609102 C 10  43609942 AGCT 10  43609990A 10  43610039 A 10  43613840 C 10  43613843 T 10  43615568 TT 10 43615622 A 10  43617416 C Chromosome Position Length Mutation ID Gene 980412493 1 COSM52975 GNAQ 9 80412518 1 COSM1463119 GNAQ 9 133738342 1COSM12631 ABL1 9 133738349 1 COSM12577 ABL1 9 133738357 1 COSM12576 ABL19 133738363 1 COSM12573 ABL1 9 133747520 1 COSM12602 ABL1 9 133747571 3COSM235737 ABL1 9 133748391 1 COSM12578 ABL1 9 133748403 1 COSM12611ABL1 9 133748414 1 COSM12605 ABL1 9 133750319 1 COSM49071 ABL1 9133750356 1 COSM12604 ABL1 9 139390779 1 COSM87862 NOTCH1 9 139390804 1COSM13070 NOTCH1 9 139390816 1 COSM12776 NOTCH1 9 139390873 1 COSM13061NOTCH1 9 139397768 1 COSM13048 NOTCH1 9 139397776 1 COSM308587 NOTCH1 9139399344 1 COSM12771 NOTCH1 9 139399350 1 COSM13053 NOTCH1 9 1393993651 COSM13042 NOTCH1 9 139399422 1 COSM12772 NOTCH1 10 43609096 1COSM29803 RET 10 43609102 1 COSM29804 RET 10 43609942 13 COSM1048 RET 1043609990 1 COSM1223553 RET 10 43610039 1 COSM976 RET 10 43613840 1COSM21338 RET 10 43613843 1 gDNA18 RET 10 43615568 3 COSM977 RET 1043615622 1 COSM963 RET 10 43617416 1 COSM965 RET Chromosome PositionMutation CDS 9 80412493 c.548G > A 9 80412518 c.523A > T 9 133738342c.742C > G 9 133738349 c.749G > A 9 133738357 c.757T > C 9 133738363c.763G > A 9 133747520 c.827A > G 9 133747571 c.878_879insGCC 9133748391 c.1052T > C 9 133748403 c.1064A > G 9 133748414 c.1075T > G 9133750319 c.1150C > A 9 133750356 c.1187A > G 9 139390779 c.7412C > A 9139390804 c.7386delC 9 139390816 c.7375C > T 9 139390873 c.7318C > T 9139397768 c.5033T > C 9 139397776 c.5025C > T 9 139399344 c.4799T > C 9139399350 c.4793G > C 9 139399365 c.4778T > C 9 139399422 c.4721T > C10  43609096 c.1852T > C 10  43609102 c.1858T > C 10  43609942c.1894_1906 > AGCT 10  43609990 c.1942G > A 10  43610039 c.1991C > A 10 43613840 c.2304G > C 10  43613843 c.2307T > A 10  43615568c.2647_2648GC > TT 10  43615622 c.2701G > A 10  43617416 c.2753T > CChromosome Position Mutation AA Mutation Type Strand Target Frequency 980412493 p.R183Q SNV − 15-35% 9 80412518 p.T175S SNV − 15-35% 9133738342 p.L248V SNV + 15-35% 9 133738349 p.G250E SNV + 15-35% 9133738357 p.Y253H SNV + 15-35% 9 133738363 p.E255K SNV + 15-35% 9133747520 p.D276G SNV + 15-35% 9 133747571 p.I293 > MP INS + 15-35% 9133748391 p.M351T SNV + 15-35% 9 133748403 p.E355G SNV + 15-35% 9133748414 p.F359V SNV + 15-35% 9 133750319 p.L384M SNV + 15-35% 9133750356 p.H396R SNV + 15-35% 9 139390779 p.S2471* SNV − 15-35% 9139390804 p.A2463fs*14 DEL − 15-35% 9 139390816 p.Q2459* SNV − 15-35% 9139390873 p.Q2440* SNV − 15-35% 9 139397768 p.L1678P SNV − 15-35% 9139397776 p.11675I SNV − 15-35% 9 139399344 p.L1600P SNV − 15-35% 9139399350 p.R1598P SNV − 15-35% 9 139399365 p.L1593P SNV − 15-35% 9139399422 p.L1574P SNV − 15-35% 10 43609096 p.C618R SNV + 15-35% 1043609102 p.C620R SNV + 15-35% 10 43609942 p.E632_T636 > SS Complex +15-35% 10 43609990 p.V648I SNV + 15-35% 10 43610039 p.A664D SNV + 15-35%10 43613840 p.E768D SNV + 15-35% 10 43613843 p.L769L SNV + genomic 1043615568 p.A883F MNV + 15-35% 10 43615622 p.E901K SNV + 15-35% 1043617416 p.M918T SNV + 15-35% Sanger CHPv2 Chromosome PositionDetection* Detection TSACP Detection TSTP Detection 9 80412493 DetectedNot Covered Detected Detected 9 80412518 Detected Not Covered DetectedDetected 9 133738342 Detected Detected Detected Not Covered 9 133738349Detected Detected Detected Not Covered 9 133738357 Detected DetectedDetected Not Covered 9 133738363 Detected Detected Detected Not Covered9 133747520 Detected Detected Detected Not Covered 9 133747571 DetectedNot Covered Detected Not Covered 9 133748391 Detected Detected DetectedNot Covered 9 133748403 Detected Detected Detected Not Covered 9133748414 Detected Detected Detected Not Covered 9 133750319 DetectedDetected Not Covered Not Covered 9 133750356 Detected Detected DetectedNot Covered 9 139390779 Detected Detected Not Covered Not Covered 9139390804 Detected Not Detected Not Covered Not Covered 9 139390816Detected Detected Not Covered Not Covered 9 139390873 Detected DetectedNot Covered Not Covered 9 139397768 Detected Detected Detected NotCovered 9 139397776 Detected Detected Detected Not Covered 9 139399344Detected Detected Detected Not Covered 9 139399350 Detected DetectedDetected Not Covered 9 139399365 Detected Detected Detected Not Covered9 139399422 Detected Detected Detected Not Covered 10 43609096 DetectedDetected Detected Not Covered 10 43609102 Detected Detected Detected NotCovered 10 43609942 Detected Detected Detected Not Covered 10 43609990Detected Detected Detected Not Covered 10 43610039 Detected Not CoveredDetected Not Covered 10 43613840 Detected Detected Detected Not Covered10 43613843 Not Covered Detected Detected Not Covered 10 43615568Detected Detected Detected Not Covered 10 43615622 Detected DetectedDetected Not Covered 10 43617416 Detected Detected Detected Not CoveredChromosome Position Reference 10 89624245 G 10 89624266 A 10 89624275 C10 89624297 A 10 89653686 A 10 89653782 A 10 89653814 C 10 89653844 A 1089653858 T 10 89653865 A 10 89685271 T 10 89685307 T 10 89685319 G 1089690805 G 10 89690818 TTA 10 89690838 A 10 89690847 G 10 89692779 A 1089692818 T 10 89692830 G 10 89692850 C 10 89692911 G 10 89692965 A 1089692980 A 10 89692993 G 10 89711855 CT 10 89711960 T 10 89711972 AGAT10 89711992 C 10 89711997 G 10 89717672 C 10 89717678 G 10 89717696 TChromosome Position Alternate 10 89624245 T 10 89624266 G 10 89624275 T10 89624297 G 10 89653686 G 10 89653782 G 10 89653814 T 10 89653844 G 1089653858 C 10 89653865 G 10 89685271 G 10 89685307 C 10 89685319 A 1089690805 A 10 89690818 T 10 89690838 C 10 89690847 A 10 89692779 G 1089692818 C 10 89692830 T 10 89692850 G 10 89692911 A 10 89692965 G 1089692980 G 10 89692993 T 10 89711855 C 10 89711960 C 10 89711972 A 1089711992 A 10 89711997 A 10 89717672 T 10 89717678 T 10 89717696 CChromosome Position Length Mutation ID Gene 10 89624245 1 COSM5298 PTEN10 89624266 1 COSM5101 PTEN 10 89624275 1 COSM5153 PTEN 10 89624297 1COSM5107 PTEN 10 89653686 1 gDNA34 PTEN 10 89653782 1 COSM5134 PTEN 1089653814 1 COSM5142 PTEN 10 89653844 1 COSM5050 PTEN 10 89653858 1COSM1349479 PTEN 10 89653865 1 COSM5129 PTEN 10 89685271 1 COSM5257 PTEN10 89685307 1 COSM5036 PTEN 10 89685319 1 COSM5916 PTEN 10 89690805 1COSM5102 PTEN 10 89690818 2 COSM4956 PTEN 10 89690838 1 COSM5205 PTEN 1089690847 1 COSM5983 PTEN 10 89692779 1 COSM5139 PTEN 10 89692818 1COSM5109 PTEN 10 89692830 1 COSM5266 PTEN 10 89692850 1 COSM5199 PTEN 1089692911 1 COSM5123 PTEN 10 89692965 1 COSM5130 PTEN 10 89692980 1COSM5144 PTEN 10 89692993 1 COSM5287 PTEN 10 89711855 1 COSM5907 PTEN 1089711960 1 COSM35406 PTEN 10 89711972 3 COSM4978 PTEN 10 89711992 1COSM5279 PTEN 10 89711997 1 COSM5072 PTEN 10 89717672 1 COSM5154 PTEN 1089717678 1 COSM5292 PTEN 10 89717696 1 COSM35849 PTEN ChromosomePosition Mutation CDS 10 89624245 c.19G > T 10 89624266 c.40A > G 1089624275 c.49C > T 10 89624297 c.71A > G 10 89653686 c.80 − 96A > G 1089653782 c.80A > G 10 89653814 c.112C > T 10 89653844 c.142A > G 1089653858 c.156T > C 10 89653865 c.163A > G 10 89685271 c.166T > G 1089685307 c.202T > C 10 89685319 c.209 + 5G > A 10 89690805 c.212G > A 1089690818 c.227_228delAT 10 89690838 c.245A > C 10 89690847 c.253+ 1G > A 10 89692779 c.263A > G 10 89692818 c.302T > C 10 89692830c.314G > T 10 89692850 c.334C > G 10 89692911 c.395G > A 10 89692965c.449A > G 10 89692980 c.464A > G 10 89692993 c.477G > T 10 89711855c.493 − 12delT 10 89711960 c.578T > C 10 89711972 c.595_597delATG 1089711992 c.610C > A 10 89711997 c.615G > A 10 89717672 c.697C > T 1089717678 c.703G > T 10 89717696 c.721T > C Mutation Target ChromosomePosition Mutation AA Type Strand Frequency 10 89624245 p.E7* SNV +15-35% 10 89624266 p.R14G SNV + 15-35% 10 89624275 p.Q17* SNV + 15-35%10 89624297 p.D24G SNV + 15-35% 10 89653686 p.(=) SNV + genomic 1089653782 p.Y27C SNV + 15-35% 10 89653814 p.P38S SNV + 15-35% 10 89653844p.N48D SNV + 15-35% 10 89653858 p.D52D SNV + 15-35% 10 89653865 p.R55GSNV + 15-35% 10 89685271 p.F56V SNV + 15-35% 10 89685307 p.Y68H SNV +15-35% 10 89685319 p.? SNV + 15-35% 10 89690805 p.C71Y SNV + 15-35% 1089690818 p.Y76fs*1 DEL + 15-35% 10 89690838 p.N82T SNV + 15-35% 1089690847 p.? SNV + 15-35% 10 89692779 p.Y88C SNV + 15-35% 10 89692818p.I101T SNV + 15-35% 10 89692830 p.C105F SNV + 15-35% 10 89692850p.L112V SNV + 15-35% 10 89692911 p.G132D SNV + 15-35% 10 89692965p.E150G SNV + 15-35% 10 89692980 p.Y155C SNV + 15-35% 10 89692993p.R159S SNV + 15-35% 10 89711855 p.? DEL + 15-35% 10 89711960 p.L193PSNV + 15-35% 10 89711972 p.M199del DEL + 15-35% 10 89711992 p.P204TSNV + 15-35% 10 89711997 p.M2051 SNV + 15-35% 10 89717672 p.R233* SNV +15-35% 10 89717678 p.E235* SNV + 15-35% 10 89717696 p.F241L SNV + 15-35%Sanger CHPv2 TSACP TSTP Chromosome Position Detection* DetectionDetection Detection 10 89624245 Detected Detected Detected Detected 1089624266 Detected Detected Detected Detected 10 89624275 DetectedDetected Detected Detected 10 89624297 Detected Detected DetectedDetected 10 89653686 Not Covered Not Covered Not Covered Detected 1089653782 Detected Not Covered Not Covered Detected 10 89653814 DetectedNot Covered Not Covered Detected 10 89653844 Detected Not Covered NotCovered Detected 10 89653858 Detected Not Covered Not Covered Detected10 89653865 Detected Not Covered Not Covered Detected 10 89685271Detected Detected Not Covered Detected 10 89685307 Detected DetectedDetected Detected 10 89685319 Detected Detected Detected Detected 1089690805 Detected Not Covered Not Covered Detected 10 89690818 DetectedNot Covered Not Covered Detected 10 89690838 Detected Not Covered NotCovered Detected 10 89690847 Detected Not Covered Not Covered Detected10 89692779 Detected Not Covered Not Covered Detected 10 89692818Detected Detected Not Covered Detected 10 89692830 Detected Detected NotCovered Detected 10 89692850 Detected Detected Not Covered Detected 1089692911 Detected Detected Not Covered Detected 10 89692965 Detected NotCovered Not Covered Detected 10 89692980 Detected Not Covered NotCovered Detected 10 89692993 Detected Not Covered Not Covered Detected10 89711855 Detected Detected Not Covered Not Detected 10 89711960Detected Not Covered Detected Detected 10 89711972 Detected Not CoveredDetected Detected 10 89711992 Detected Not Covered Detected Detected 1089711997 Detected Not Covered Detected Detected 10 89717672 DetectedDetected Detected Detected 10 89717678 Detected Detected DetectedDetected 10 89717696 Detected Detected Detected Detected ChromosomePosition Reference 10 89717762 A 10 89717769 TA 10 89720728 A 1089720744 G 10 89720798 GTACT 10 89720874 A 10 89720907 T 10 89725042 A10 89725056 TTC 10 89725072 A 10 89725108 C 10 123258034 A 10 123274774A 10 123274794 T 10 123274810 T 10 123279503 T 10 123279519 C 10123279677 G 11 533874 T 11 533881 C 11 534242 A 11 534288 C 11 108117798C 11 108119823 T 11 108123551 C 11 108123641 T 11 108138003 T 11108155132 G 11 108170479 G 11 108170587 C 11 108172374 G 11 108172385 C11 108172421 G Chromosome Position Alternate 10 89717762 T 10 89717769 T10 89720728 G 10 89720744 T 10 89720798 G 10 89720874 G 10 89720907 G 1089725042 G 10 89725056 T 10 89725072 G 10 89725108 G 10 123258034 T 10123274774 G 10 123274794 C 10 123274810 C 10 123279503 C 10 123279519 T10 123279677 C 11 533874 C 11 533881 T 11 534242 G 11 534288 A 11108117798 T 11 108119823 C 11 108123551 T 11 108123641 A 11 108138003 C11 108155132 A 11 108170479 T 11 108170587 G 11 108172374 T 11 108172385T 11 108172421 C Chromosome Position Length Mutation ID Gene 10 897177621 COSM43075 PTEN 10 89717769 1 COSM5809 PTEN 10 89720728 1 COSM1349606PTEN 10 89720744 1 COSM5312 PTEN 10 89720798 4 COSM4958 PTEN 10 897208741 COSM1349625 PTEN 10 89720907 1 gDNA19 PTEN 10 89725042 1 COSM5966 PTEN10 89725056 2 COSM4936 PTEN 10 89725072 1 COSM1349633 PTEN 10 89725108 1COSM23645 PTEN 10 123258034 1 COSM36912 FGFR2 10 123274774 1 COSM36906FGFR2 10 123274794 1 COSM36904 FGFR2 10 123274810 1 COSM1346272 FGFR2 10123279503 1 COSM36901 FGFR2 10 123279519 1 COSM29824 FGFR2 10 1232796771 COSM36903 FGFR2 11 533874 1 COSM499 HRAS 11 533881 1 COSM495 HRAS 11534242 1 gDNA20, COSM249860 HRAS 11 534288 1 COSM483 HRAS 11 108117798 1COSM21323 ATM 11 108119823 1 COSM21825 ATM 11 108123551 1 COSM22499 ATM11 108123641 1 COSM1158828 ATM 11 108138003 1 COSM21826 ATM 11 1081551321 COSM22507 ATM 11 108170479 1 COSM21920 ATM 11 108170587 1 COSM218294ATM 11 108172374 1 COSM49005 ATM 11 108172385 1 COSM172204 ATM 11108172421 1 COSM21918 ATM Chromosome Position Mutation CDS 10 89717762c.787A > T 10 89717769 c.800delA 10 89720728 c.879A > G 10 89720744c.895G > T 10 89720798 c.955_958delACTT 10 89720874 c.1025A > G 1089720907 c.1026 + 32T > G 10 89725042 c.1027 − 2A > G 10 89725056c.1040_1041delTC 10 89725072 c.1055A > G 10 89725108 c.1091C > G 10123258034 c.1647T > A 10 123274774 c.1144T > C 10 123274794 c.1124A > G10 123274810 c.1108A > G 10 123279503 c.929A > G 10 123279519 c.913G > A10 123279677 c.755C > G 11 533874 c.182A > G 11 533881 c.175G > A 11534242 c.81T > C 11 534288 c.35G > T 11 108117798 c.1009C > T 11108119823 c.1229T > C 11 108123551 c.1810C > T 11 108123641 c.1898+ 2T > A 11 108138003 c.2572T > C 11 108155132 c.3925G > A 11 108170479c.5044G > T 11 108170587 c.5152C > G 11 108172374 c.5178 − 1G > T 11108172385 c.5188C > T 11 108172421 c.5224G > C Mutation TargetChromosome Position Mutation AA Type Strand Frequency 10 89717762p.K263* SNV + 15-35%  10 89717769 p.K267fs*9 DEL + 15-35%  10 89720728p.G293G SNV + 15-35%  10 89720744 p.E299* SNV + 15-35%  10 89720798p.T319fs*1 DEL + 15-35%  10 89720874 p.K342R SNV + 15-35%  10 89720907p.(=) SNV + genomic 10 89725042 p.? SNV + 15-35%  10 89725056p.F347fs*13 DEL + 15-35%  10 89725072 p.E352G SNV + 15-35%  10 89725108p.S364C SNV + 15-35%  10 123258034 p.N549K SNV − 5-15% 10 123274774p.C382R SNV − 5-15% 10 123274794 p.Y375C SNV − 5-15% 10 123274810p.T370A SNV − 5-15% 10 123279503 p.K310R SNV − 5-15% 10 123279519p.G305R SNV − 5-15% 10 123279677 p.S252W SNV − 5-15% 11 533874 p.Q61RSNV − 5-15% 11 533881 p.A59T SNV − 5-15% 11 534242 p.H27H SNV − genomic11 534288 p.G12V SNV − 5-15% 11 108117798 p.R337C SNV + 5-15% 11108119823 p.V410A SNV + 5-15% 11 108123551 p.P604S SNV + 5-15% 11108123641 p.? SNV + 5-15% 11 108138003 p.F858L SNV + 5-15% 11 108155132p.A1309T SNV + 5-15% 11 108170479 p.D1682Y SNV + 5-15% 11 108170587p.L1718V SNV + 5-15% 11 108172374 p.? SNV + 5-15% 11 108172385 p.R1730*SNV + 5-15% 11 108172421 p.A1742P SNV + 5-15% Sanger CHPv2 TSACP TSTPChromosome Position Detection* Detection Detection Detection 10 89717762Detected Detected Detected Detected 10 89717769 Detected DetectedDetected Detected 10 89720728 Detected Detected Detected Not Covered 1089720744 Detected Detected Detected Not Covered 10 89720798 DetectedDetected Detected Not Covered 10 89720874 Detected Detected Detected NotCovered 10 89720907 Not Covered Not Covered Detected Not Covered 1089725042 Detected Not Covered Not Covered Detected 10 89725056 DetectedNot Covered Not Covered Detected 10 89725072 Detected Not Covered NotCovered Detected 10 89725108 Detected Not Covered Not Covered Detected10 123258034 Detected Detected Detected Not Covered 10 123274774Detected Detected Detected Not Covered 10 123274794 Detected DetectedDetected Not Covered 10 123274810 Detected Detected Detected Not Covered10 123279503 Detected Detected Detected Detected 10 123279519 DetectedDetected Detected Detected 10 123279677 Detected Detected DetectedDetected 11 533874 Detected Detected Detected Not Covered 11 533881Detected Detected Detected Not Covered 11 534242 Not Covered DetectedNot Covered Not Covered 11 534288 Detected Detected Detected Not Covered11 108117798 Detected Detected Not Covered Not Covered 11 108119823Detected Detected Detected Not Covered 11 108123551 Detected DetectedDetected Not Covered 11 108123641 Detected Not Covered Detected NotCovered 11 108138003 Detected Detected Detected Not Covered 11 108155132Detected Detected Not Detected Not Covered 11 108170479 DetectedDetected Detected Not Covered 11 108170587 Detected Not Covered DetectedNot Covered 11 108172374 Detected Detected Not Covered Not Covered 11108172385 Detected Detected Not Covered Not Covered 11 108172421Detected Detected Detected Not Covered Chromosome Position Reference 11108173640 C 11 108173736 T 11 108180945 G 11 108200958 A 11 108204681 A11 108205769 G 11 108205780 C 11 108206594 A 11 108218045 A 11 108218089C 11 108218196 T 11 108225590 A 11 108225661 A 11 108236087 G 11108236118 A 11 108236203 C 12 25362805 C 12 25378647 T 12 25380275 T 1225380283 C 12 25398207 C 12 25398215 G 12 25398284 C 12 25398295 T 12112888165 G 12 112888189 G 12 112888199 C 12 112888210 G 12 112926852 C12 112926888 G 12 112926899 A 12 112926908 C 12 121431413 G ChromosomePosition Alternate 11 108173640 T 11 108173736 G 11 108180945 C 11108200958 C 11 108204681 G 11 108205769 C 11 108205780 A 11 108206594 T11 108218045 G 11 108218089 G 11 108218196 C 11 108225590 T 11 108225661G 11 108236087 A 11 108236118 G 11 108236203 T 12 25362805 T 12 25378647G 12 25380275 G 12 25380283 T 12 25398207 A 12 25398215 A 12 25398284 T12 25398295 C 12 112888165 T 12 112888189 A 12 112888199 T 12 112888210A 12 112926852 T 12 112926888 C 12 112926899 G 12 112926908 A 12121431413 T Chromosome Position Length Mutation ID Gene 11 108173640 1COSM12792 ATM 11 108173736 1 COSM1183962 ATM 11 108180945 1 COSM21922ATM 11 108200958 1 COSM12951 ATM 11 108204681 1 COSM12791 ATM 11108205769 1 COSM21636 ATM 11 108205780 1 COSM1235404 ATM 11 108206594 1COSM22481 ATM 11 108218045 1 COSM1183939 ATM 11 108218089 1 COSM22485ATM 11 108218196 1 gDNA21 ATM 11 108225590 1 COSM21930 ATM 11 1082256611 gDNA22 ATM 11 108236087 1 COSM21626 ATM 11 108236118 1 COSM1351060 ATM11 108236203 1 COSM21624 ATM 12 25362805 1 COSM41307 KRAS 12 25378647 1COSM19940 KRAS 12 25380275 1 COSM554 KRAS 12 25380283 1 COSM546 KRAS 1225398207 1 AMXsynt11 KRAS 12 25398215 1 COSM14208 KRAS 12 25398284 1COSM521 KRAS 12 25398295 1 COSM507 KRAS 12 112888165 1 COSM13011 PTPN1112 112888189 1 COSM13013 PTPN11 12 112888199 1 COSM13015 PTPN11 12112888210 1 COSM13000 PTPN11 12 112926852 1 COSM13034 PTPN11 12112926888 1 COSM13027 PTPN11 12 112926899 1 COSM1358900 PTPN11 12112926908 1 COSM13031 PTPN11 12 121431413 1 COSM21471 HNF1A ChromosomePosition Mutation CDS 11 108173640 c.5380C > T 11 108173736 c.5476T > G11 108180945 c.5821G > C 11 108200958 c.7325A > C 11 108204681c.7996A > G 11 108205769 c.8084G > C 11 108205780 c.8095C > A 11108206594 c.8174A > T 11 108218045 c.8624A > G 11 108218089 c.8668C > G11 108218196 c.8671 + 104T > C 11 108225590 c.8839A > T 11 108225661c.8850 + 60A > G 11 108236087 c.9023G > A 11 108236118 c.9054A > G 11108236203 c.9139C > T 12 25362805 c.491G > A 12 25378647 c.351A > C 1225380275 c.183A > C 12 25380283 c.175G > A 12 25398207 c.111 + 1C > T 1225398215 c.104C > T 12 25398284 c.35G > A 12 25398295 c.24A > G 12112888165 c.181G > T 12 112888189 c.205G > A 12 112888199 c.215C > T 12112888210 c.226G > A 12 112926852 c.1472C > T 12 112926888 c.1508G > C12 112926899 c.1519A > G 12 112926908 c.1528C > A 12 121431413c.617G > T Mutation Target Chromosome Position Mutation AA Type StrandFrequency 11 108173640 p.L1794L SNV + 5-15% 11 108173736 p.L1826V SNV +5-15% 11 108180945 p.V1941L SNV + 5-15% 11 108200958 p.Q2442P SNV +5-15% 11 108204681 p.T2666A SNV + 5-15% 11 108205769 p.G2695A SNV +5-15% 11 108205780 p.P2699T SNV + 5-15% 11 108206594 p.D2725V SNV +5-15% 11 108218045 p.N2875S SNV + 5-15% 11 108218089 p.L2890V SNV +5-15% 11 108218196 p.(=) SNV + genomic 11 108225590 p.T2947S SNV + 5-15%11 108225661 p.(=) SNV + genomic 11 108236087 p.R3008H SNV + 5-15% 11108236118 p.K3018K SNV + 5-15% 11 108236203 p.R3047* SNV + 5-15% 1225362805 p.R164Q SNV − 5-15% 12 25378647 p.K117N SNV − 5-15% 12 25380275p.Q61H SNV − 5-15% 12 25380283 p.A59T SNV − 5-15% 12 25398207 p.? SNV −5-15% 12 25398215 p.T35I SNV − 5-15% 12 25398284 p.G12D SNV − 5-15% 1225398295 p.V8V SNV − 5-15% 12 112888165 p.D61Y SNV + 5-15% 12 112888189p.E69K SNV + 5-15% 12 112888199 p.A72V SNV + 5-15% 12 112888210 p.E76KSNV + 5-15% 12 112926852 p.P491L SNV + 5-15% 12 112926888 p.G503A SNV +5-15% 12 112926899 p.T507A SNV + 5-15% 12 112926908 p.Q510K SNV + 5-15%12 121431413 p.W206L SNV + 5-15% Sanger CHPv2 TSACP TSTP ChromosomePosition Detection* Detection Detection Detection 11 108173640 DetectedDetected Detected Not Covered 11 108173736 Detected Not Covered DetectedNot Covered 11 108180945 Detected Detected Detected Not Covered 11108200958 Detected Detected Detected Not Covered 11 108204681 DetectedDetected Detected Not Covered 11 108205769 Detected Detected DetectedNot Covered 11 108205780 Detected Detected Detected Not Covered 11108206594 Detected Detected Detected Not Covered 11 108218045 DetectedDetected Not Covered Not Covered 11 108218089 Detected Detected DetectedNot Covered 11 108218196 Not Covered Not Covered Detected Not Covered 11108225590 Detected Detected Detected Not Covered 11 108225661 NotCovered Not Covered Detected Not Covered 11 108236087 Detected DetectedDetected Not Covered 11 108236118 Detected Detected Detected Not Covered11 108236203 Detected Detected Detected Not Covered 12 25362805 DetectedNot Covered Not Covered Detected 12 25378647 Detected Detected DetectedDetected 12 25380275 Detected Detected Detected Detected 12 25380283Detected Detected Detected Detected 12 25398207 Detected Detected NotCovered Detected 12 25398215 Detected Detected Not Covered Detected 1225398284 Detected Detected Detected Detected 12 25398295 DetectedDetected Detected Detected 12 112888165 Detected Detected Detected NotCovered 12 112888189 Detected Detected Detected Not Covered 12 112888199Detected Detected Detected Not Covered 12 112888210 Detected DetectedDetected Not Covered 12 112926852 Detected Detected Not Covered NotCovered 12 112926888 Detected Detected Detected Not Covered 12 112926899Detected Detected Detected Not Covered 12 112926908 Detected DetectedDetected Not Covered 12 121431413 Detected Detected Detected Not CoveredChromosome Position Reference 12 121431428 A 12 121431481 C 12 121431506A 12 121432032 C 12 121432040 C 12 121432117 G 12 121432117 G 1328592629 T 13 28592642 C 13 28592653 C 13 28602329 G 13 28608255 G 1328608281 A 13 28610138 G 13 28610183 A 13 48919244 G 13 48923148 T 1348941628 A 13 48941648 C 13 48941658 A 13 48941672 A 13 48942685 C 1348953760 C 13 48955538 C 13 48955550 C 13 48955571 T 13 49027168 C 1349027249 T 13 49033890 TAGAACATATCATC (SEQ ID NO: 29) 13 49033916 C 1349033926 T 13 49037865 A 13 49037877 G Chromosome Position Alternate 12121431428 C 12 121431481 T 12 121431506 G 12 121432032 T 12 121432040 T12 121432117 GC 12 121432117 C 13 28592629 C 13 28592642 A 13 28592653 T13 28602329 A 13 28608255 GATCATATTCATATTCTCTGAA (SEQ ID NO: 30) 1328608281 G 13 28610138 A 13 28610183 G 13 48919244 T 13 48923148 A 1348941628 T 13 48941648 T 13 48941658 G 13 48941672 G 13 48942685 T 1348953760 T 13 48955538 T 13 48955550 T 13 48955571 C 13 49027168 T 1349027249 C 13 49033890 T 13 49033916 T 13 49033926 C 13 49037865 G 1349037877 T Chromosome Position Length Mutation ID Gene 12 121431428 1COSM24900 HNF1A 12 121431481 1 COSM24832 HNF1A 12 121431506 1 COSM21474HNF1A 12 121432032 1 COSM24923 HNF1A 12 121432040 1 COSM24692 HNF1A 12121432117 1 COSM21481 HNF1A 12 121432117 1 gDNA23 HNF1A 13 28592629 1COSM1166729 FLT3 13 28592642 1 COSM783 FLT3 13 28592653 1 COSM25248 FLT313 28602329 1 COSM786 FLT3 13 28608255 21 COSM27907 FLT3 13 28608281 1COSM19522 FLT3 13 28610138 1 COSM28042 FLT3 13 28610183 1 gDNA24 FLT3 1348919244 1 COSM890 RB1 13 48923148 1 COSM915 RB1 13 48941628 1 COSM28816RB1 13 48941648 1 COSM891 RB1 13 48941658 1 COSM1367204 RB1 13 489416721 COSM1367206 RB1 13 48942685 1 COSM879 RB1 13 48953760 1 COSM895 RB1 1348955538 1 COSM887 RB1 13 48955550 1 COSM888 RB1 13 48955571 1COSM1367255 RB1 13 49027168 1 COSM892 RB1 13 49027249 1 COSM35483 RB1 1349033890 13 COSM870 RB1 13 49033916 1 COSM13117 RB1 13 49033926 1COSM942 RB1 13 49037865 1 COSM1042 RB1 13 49037877 1 COSM883 RB1Chromosome Position Mutation CDS 12 121431428 c.632A > C 12 121431481c.685C > T 12 121431506 c.710A > G 12 121432032 c.779C > T 12 121432040c.787C > T 12 121432117 c.872_873insC 12 121432117 c.864G > C 1328592629 c.2516A > G 13 28592642 c.2503G > T 13 28592653 c.2492G > A 1328602329 c.2039C > T 13 28608255 c.1800_1801insTTCAGAGAATATGAATATGAT(SEQ ID NO: 31) 13 28608281 c.1775T > C 13 28610138 c.1352C > T 1328610183 c.1310 − 3T > C 13 48919244 c.409G > T 13 48923148 c.596T > A13 48941628 c.940 − 2A > T 13 48941648 c.958C > T 13 48941658 c.968A > G13 48941672 c.982A > G 13 48942685 c.1072C > T 13 48953760 c.1363C > T13 48955538 c.1654C > T 13 48955550 c.1666C > T 13 48955571 c.1687T > C13 49027168 c.1735C > T 13 49027249 c.1814 + 2T > C 13 49033890c.2028_2040del13 13 49033916 c.2053C > T 13 49033926 c.2063T > C 1349037865 c.2107 − 2A > G 13 49037877 c.2117G > T Mutation Target SangerChromosome Position Mutation AA Type Strand Frequency Detection* 12121431428 p.Q211P SNV + 5-15% Detected 12 121431481 p.R229* SNV + 5-15%Detected 12 121431506 p.N237S SNV + 5-15% Detected 12 121432032 p.T260MSNV + 5-15% Detected 12 121432040 p.R263C SNV + 5-15% Detected 12121432117 p.G292fs*25 INS + 5-15% Detected 12 121432117 p.G288G SNV +genomic Not Covered 13 28592629 p.D839G SNV − 5-15% Detected 13 28592642p.D835Y SNV − 5-15% Detected 13 28592653 p.G831E SNV − 5-15% Detected 1328602329 p.A680V SNV − 5-15% Detected 13 28608255 p.D600_L60linsFREYEYDINS − 5-15% Detected 13 28608281 p.V592A SNV − 5-15% Detected 1328610138 p.S451F SNV − 5-15% Detected 13 28610183 p.? SNV − genomic NotCovered 13 48919244 p.E137* SNV + 5-15% Detected 13 48923148 p.L199*SNV + 5-15% Detected 13 48941628 p.? SNV + 5-15% Detected 13 48941648p.R320* SNV + 5-15% Detected 13 48941658 p.E323G SNV + 5-15% Detected 1348941672 p.N328D SNV + 5-15% Detected 13 48942685 p.R358* SNV + 5-15%Detected 13 48953760 p.R455* SNV + 5-15% Detected 13 48955538 p.R552*SNV + 5-15% Detected 13 48955550 p.R556* SNV + 5-15% Detected 1348955571 p.W563R SNV + 5-15% Detected 13 49027168 p.R579* SNV + 5-15%Detected 13 49027249 p.? SNV + 5-15% Detected 13 49033890 p.L676fs*16DEL + 5-15% Detected 13 49033916 p.Q685* SNV + 5-15% Detected 1349033926 p.L688P SNV + 5-15% Detected 13 49037865 p.? SNV + 5-15%Detected 13 49037877 p.C706F SNV + 5-15% Detected CHPv2 TSACP TSTPChromosome Position Detection Detection Detection 12 121431428 DetectedDetected Not Covered 12 121431481 Not Covered Detected Not Covered 12121431506 Not Covered Detected Not Covered 12 121432032 Detected NotCovered Not Covered 12 121432040 Detected Not Covered Not Covered 12121432117 Not Covered Detected Not Covered 12 121432117 Not CoveredDetected Not Covered 13 28592629 Detected Detected Not Covered 1328592642 Detected Detected Not Covered 13 28592653 Detected Detected NotCovered 13 28602329 Detected Detected Not Covered 13 28608255 NotDetected Not Detected Not Covered 13 28608281 Detected Detected NotCovered 13 28610138 Detected Detected Not Covered 13 28610183 DetectedDetected Not Covered 13 48919244 Detected Detected Not Covered 1348923148 Detected Detected Not Covered 13 48941628 Detected Not CoveredNot Covered 13 48941648 Detected Not Covered Not Covered 13 48941658Detected Not Covered Not Covered 13 48941672 Detected Not Covered NotCovered 13 48942685 Detected Detected Not Covered 13 48953760 DetectedNot Covered Not Covered 13 48955538 Detected Detected Not Covered 1348955550 Detected Detected Not Covered 13 48955571 Detected Detected NotCovered 13 49027168 Detected Detected Not Covered 13 49027249 NotCovered Detected Not Covered 13 49033890 Detected Detected Not Covered13 49033916 Detected Detected Not Covered 13 49033926 Detected DetectedNot Covered 13 49037865 Detected Detected Not Covered 13 49037877Detected Detected Not Covered Chromosome Position Reference 13 49037903A 13 49037913 A 13 49039164 G 13 49039183 T 13 49039189 A 13 49039215 A14 105246551 C 15 66727455 G 15 66727483 G 15 90631838 C 15 90631879 T15 90631934 C 16 68835650 GGTGTGATTACAGTCAAAAGGCCTCTACGGT (SEQ ID NO:32) 16 68846087 A 16 68846137 G 16 68847282 G 16 68855924 A 16 68855934T 16 68855966 G 16 68856041 G 16 68856093 C 16 68856105 G 17 7572962 GT17 7572986 G 17 7573010 T 17 7574003 G 17 7574012 C 17 7574018 G 177574026 C 17 7576855 G 17 7576865 A 17 7576883 T 17 7576897 G ChromosomePosition Alternate 13 49037903 T 13 49037913 G 13 49039164 T 13 49039183G 13 49039189 G 13 49039215 T 14 105246551 T 15 66727455 T 15 66727483 A15 90631838 T 15 90631879 C 15 90631934 T 16 68835650 G 16 68846087 G 1668846137 C 16 68847282 A 16 68855924 AC 16 68855934 C 16 68855966 A 1668856041 A 16 68856093 T 16 68856105 A 17 7572962 G 17 7572986 A 177573010 C 17 7574003 A 17 7574012 A 17 7574018 A 17 7574026 A 17 7576855A 17 7576865 C 17 7576883 C 17 7576897 A Chromosome Position LengthMutation ID Gene 13 49037903 1 COSM940 RB1 13 49037913 1 COSM1367309 RB113 49039164 1 COSM868 RB1 13 49039183 1 COSM916 RB1 13 49039189 1COSM551465 RB1 13 49039215 1 COSM254910 RB1 14 105246551 1 COSM33765AKT1 15 66727455 1 COSM1235478 MAP2K1 15 66727483 1 COSM1235479 MAP2K115 90631838 1 COSM33733 IDH2 15 90631879 1 COSM1375400 IDH2 15 906319341 COSM41590 IDH2 16 68835650 30 AMXsynt10 CDH1 16 68846087 1 COSM1379165CDH1 16 68846137 1 COSM19748 CDH1 16 68847282 1 COSM19750 CDH1 1668855924 1 COSM25267 CDH1 16 68855934 1 COSM19746 CDH1 16 68855966 1COSM19758 CDH1 16 68856041 1 COSM19743 CDH1 16 68856093 1 COSM19822 CDH116 68856105 1 COSM19418 CDH1 17 7572962 1 COSM13747 TP53 17 7572986 1COSM307348 TP53 17 7573010 1 COSM1191161 TP53 17 7574003 1 COSM11073TP53 17 7574012 1 COSM11286 TP53 17 7574018 1 COSM11071 TP53 17 75740261 COSM11514 TP53 17 7576855 1 COSM11354 TP53 17 7576865 1 COSM44823 TP5317 7576883 1 COSM46088 TP53 17 7576897 1 COSM10786 TP53 ChromosomePosition Mutation CDS 13 49037903 c.2143A > T 13 49037913 c.2153A > G 1349039164 c.2242G > T 13 49039183 c.2261T > G 13 49039189 c.2267A > G 1349039215 c.2293A > T 14 105246551 c.49G > A 15 66727455 c.171G > T 1566727483 c.199G > A 15 90631838 c.515G > A 15 90631879 c.474A > G 1590631934 c.419G > A 16 68835650 c.241del30 16 68846087 c.1058A > G 1668846137 c.1108G > C 16 68847282 c.1204G > A 16 68855924 c.1733_1734insC16 68855934 c.1742T > C 16 68855966 c.1774G > A 16 68856041 c.1849G > A16 68856093 c.1901C > T 16 68856105 c.1913G > A 17 7572962 c.1146delA 177572986 c.1123C > T 17 7573010 c.1101 − 2A > G 17 7574003 c.1024C > T 177574012 c.1015G > T 17 7574018 c.1009C > T 17 7574026 c.1001G > T 177576855 c.991C > T 17 7576865 c.981T > G 17 7576883 c.963A > G 177576897 c.949C > T Mutation Target Sanger Chromosome Position MutationAA Type Strand Frequency Detection* 13 49037903 p.K715* SNV + 5-15%Detected 13 49037913 p.D718G SNV + 5-15% Detected 13 49039164 p.E748*SNV + 5-15% Detected 13 49039183 p.V754G SNV + 5-15% Detected 1349039189 p.Y756C SNV + 5-15% Detected 13 49039215 p.K765* SNV + 5-15%Detected 14 105246551 p.E17K SNV − 5-15% Detected 15 66727455 p.K57NSNV + 5-15% Detected 15 66727483 p.D67N SNV + 5-15% Detected 15 90631838p.R172K SNV − 5-15% Detected 15 90631879 p.P158P SNV − 5-15% Detected 1590631934 p.R140Q SNV − 5-15% Detected 16 68835650 p.G81_F91del DEL +5-15% Detected 16 68846087 p.E353G SNV + 5-15% Detected 16 68846137p.D370H SNV + 5-15% Detected 16 68847282 p.D402N SNV + 5-15% Detected 1668855924 p.G579fs*9 INS + 5-15% Detected 16 68855934 p.L581P SNV + 5-15%Detected 16 68855966 p.A592T SNV + 5-15% Detected 16 68856041 p.A617TSNV + 5-15% Detected 16 68856093 p.A634V SNV + 5-15% Detected 1668856105 p.W638* SNV + 5-15% Detected 17 7572962 p.K382fs* > 12 DEL −5-15% Detected 17 7572986 p.Q375* SNV − 5-15% Detected 17 7573010 p.?SNV − 5-15% Detected 17 7574003 p.R342* SNV − 5-15% Detected 17 7574012p.E339* SNV − 5-15% Detected 17 7574018 p.R337C SNV − 5-15% Detected 177574026 p.G334V SNV − 5-15% Detected 17 7576855 p.Q331* SNV − 5-15%Detected 17 7576865 p.Y327* SNV − 5-15% Detected 17 7576883 p.K321K SNV− 5-15% Detected 17 7576897 p.Q317* SNV − 5-15% Detected CHPv2 TSACPTSTP Chromosome Position Detection Detection Detection 13 49037903Detected Detected Not Covered 13 49037913 Detected Detected Not Covered13 49039164 Detected Detected Not Covered 13 49039183 Detected DetectedNot Covered 13 49039189 Detected Detected Not Covered 13 49039215Detected Detected Not Covered 14 105246551 Detected Detected Detected 1566727455 Not Covered Not Covered Detected 15 66727483 Not Covered NotCovered Detected 15 90631838 Detected Not Covered Not Covered 1590631879 Detected Not Covered Not Covered 15 90631934 Detected NotCovered Not Covered 16 68835650 Not Detected Not Detected Not Covered 1668846087 Detected Not Covered Detected 16 68846137 Detected DetectedDetected 16 68847282 Detected Detected Detected 16 68855924 Not CoveredNot Covered Detected 16 68855934 Not Covered Not Covered Detected 1668855966 Not Covered Not Covered Detected 16 68856041 Not Covered NotCovered Detected 16 68856093 Not Covered Not Covered Detected 1668856105 Not Covered Not Covered Detected 17 7572962 Not Covered NotCovered Detected 17 7572986 Not Covered Not Covered Detected 17 7573010Not Covered Not Covered Detected 17 7574003 Detected Detected Detected17 7574012 Detected Detected Detected 17 7574018 Detected DetectedDetected 17 7574026 Detected Detected Detected 17 7576855 Not CoveredNot Covered Detected 17 7576865 Not Covered Not Covered Detected 177576883 Not Covered Not Covered Detected 17 7576897 Not Covered NotCovered Detected Chromosome Position Reference 17 7577022 G 17 7577046 C17 7577105 G 17 7577120 C 17 7577538 C 17 7577548 C 17 7577559 G 177577580 T 17 7578115 T 17 7578190 T 17 7578196 A 17 7578203 C 17 7578235T 17 7578388 C 17 7578442 T 17 7578449 C 17 7578461 C 17 7578526 C 177578535 T 17 7578542 G 17 7578550 G 17 7579295 C 17 7579312 C 17 7579358C 17 7579368 A 17 7579414 C 17 7579442 G 17 7579472 G 17 7579521 C 177579536 C 17 7579553 A 17 7579575 G 17 7579715 AG Chromosome PositionAlternate 17 7577022 A 17 7577046 A 17 7577105 A 17 7577120 T 17 7577538T 17 7577548 T 17 7577559 A 17 7577580 C 17 7578115 C 17 7578190 C 177578196 T 17 7578203 T 17 7578235 C 17 7578388 T 17 7578442 C 17 7578449T 17 7578461 A 17 7578526 T 17 7578535 C 17 7578542 C 17 7578550 A 177579295 T 17 7579312 T 17 7579358 A 17 7579368 C 17 7579414 T 17 7579442A 17 7579472 C 17 7579521 A 17 7579536 A 17 7579553 G 17 7579575 A 177579715 A Chromosome Position Length Mutation ID Gene 17 7577022 1COSM10663 TP53 17 7577046 1 COSM10710 TP53 17 7577105 1 COSM10863 TP5317 7577120 1 COSM10660 TP53 17 7577538 1 COSM10662 TP53 17 7577548 1COSM6932 TP53 17 7577559 1 COSM10812 TP53 17 7577580 1 COSM10725 TP53 177578115 1 gDNA25 TP53 17 7578190 1 COSM10758 TP53 17 7578196 1 COSM44317TP53 17 7578203 1 COSM10667 TP53 17 7578235 1 COSM43947 TP53 17 75783881 COSM10738 TP53 17 7578442 1 COSM10808 TP53 17 7578449 1 COSM10739 TP5317 7578461 1 COSM10670 TP53 17 7578526 1 COSM10801 TP53 17 7578535 1COSM11582 TP53 17 7578542 1 COSM11462 TP53 17 7578550 1 COSM44226 TP5317 7579295 1 COSM44985 TP53 17 7579312 1 COSM43904 TP53 17 7579358 1COSM10716 TP53 17 7579368 1 COSM46103 TP53 17 7579414 1 COSM44492 TP5317 7579442 1 COSM43910 TP53 17 7579472 1 gDNA26, COSM250061 TP53 177579521 1 COSM12168 TP53 17 7579536 1 COSM44907 TP53 17 7579553 1COSM43664 TP53 17 7579575 1 COSM46286 TP53 17 7579715 1 COSM85573 TP53Chromosome Position Mutation CDS 17 7577022 c.916C > T 17 7577046c.892G > T 17 7577105 c.833C > T 17 7577120 c.818G > A 17 7577538c.743G > A 17 7577548 c.733G > A 17 7577559 c.722C > T 17 7577580c.701A > G 17 7578115 c.672 + 62A > G 17 7578190 c.659A > G 17 7578196c.653T > A 17 7578203 c.646G > A 17 7578235 c.614A > G 17 7578388c.542G > A 17 7578442 c.488A > G 17 7578449 c.481G > A 17 7578461c.469G > T 17 7578526 c.404G > A 17 7578535 c.395A > G 17 7578542c.388C > G 17 7578550 c.380C > T 17 7579295 c.375 + 17G > A 17 7579312c.375G > A 17 7579358 c.329G > T 17 7579368 c.319T > G 17 7579414c.273G > A 17 7579442 c.245C > T 17 7579472 c.215G > C 17 7579521c.166G > T 17 7579536 c.151G > T 17 7579553 c.134T > C 17 7579575c.112C > T 17 7579715 c.80delC Mutation Target Sanger ChromosomePosition Mutation AA Type Strand Frequency Detection* 17 7577022 p.R306*SNV − 5-15% Detected 17 7577046 p.E298* SNV − 5-15% Detected 17 7577105p.P278L SNV − 5-15% Detected 17 7577120 p.R273H SNV − 5-15% Detected 177577538 p.R248Q SNV − 5-15% Detected 17 7577548 p.G245S SNV − 5-15%Detected 17 7577559 p.S241F SNV − 5-15% Detected 17 7577580 p.Y234C SNV− 5-15% Detected 17 7578115 p.(=) SNV − genomic Not Covered 17 7578190p.Y220C SNV − 5-15% Detected 17 7578196 p.V218E SNV − 5-15% Detected 177578203 p.V216M SNV − 5-15% Detected 17 7578235 p.Y205C SNV − 5-15%Detected 17 7578388 p.R181H SNV − 5-15% Detected 17 7578442 p.Y163C SNV− 5-15% Detected 17 7578449 p.A161T SNV − 5-15% Detected 17 7578461p.V157F SNV − 5-15% Detected 17 7578526 p.C135Y SNV − 5-15% Detected 177578535 p.K132R SNV − 5-15% Detected 17 7578542 p.L130V SNV − 5-15%Detected 17 7578550 p.S127F SNV − 5-15% Detected 17 7579295 p.? SNV −5-15% Detected 17 7579312 p.T125T SNV − 5-15% Detected 17 7579358p.R110L SNV − 5-15% Detected 17 7579368 p.Y107D SNV − 5-15% Detected 177579414 p.W91* SNV − 5-15% Detected 17 7579442 p.P82L SNV − 5-15%Detected 17 7579472 p.R72P SNV − genomic Not Covered 17 7579521 p.E56*SNV − 5-15% Detected 17 7579536 p.E51* SNV − 5-15% Detected 17 7579553p.L45P SNV − 5-15% Detected 17 7579575 p.Q38* SNV − 5-15% Detected 177579715 p.P27fs*17 DEL − 5-15% Detected CHPv2 TSACP TSTP ChromosomePosition Detection Detection Detection 17 7577022 Detected DetectedDetected 17 7577046 Detected Detected Detected 17 7577105 DetectedDetected Detected 17 7577120 Detected Detected Detected 17 7577538Detected Detected Detected 17 7577548 Detected Detected Detected 177577559 Detected Detected Detected 17 7577580 Detected Detected Detected17 7578115 Not Covered Detected Not Covered 17 7578190 Detected DetectedDetected 17 7578196 Detected Detected Detected 17 7578203 DetectedDetected Detected 17 7578235 Detected Detected Detected 17 7578388Detected Detected Detected 17 7578442 Detected Detected Detected 177578449 Detected Detected Detected 17 7578461 Detected Detected Detected17 7578526 Detected Detected Detected 17 7578535 Detected DetectedDetected 17 7578542 Detected Detected Detected 17 7578550 DetectedDetected Detected 17 7579295 Not Covered Not Covered Not Detected 177579312 Not Covered Not Covered Detected 17 7579358 Detected DetectedDetected 17 7579368 Detected Detected Detected 17 7579414 DetectedDetected Detected 17 7579442 Detected Detected Detected 17 7579472Detected Detected Detected 17 7579521 Not Covered Not Covered Detected17 7579536 Not Covered Not Covered Detected 17 7579553 Not Covered NotCovered Detected 17 7579575 Not Covered Not Covered Detected 17 7579715Not Covered Not Covered Detected Chromosome Position Reference 177579801 G 17 37880220 T 17 37880261 G 17 37880981 A 17 37881332 G 1737881378 A 17 37881440 C 18 48575112 T 18 48575183 T 18 48575195 C 1848575209 C 18 48575671 C 18 48581198 G 18 48581229 C 18 48581243 C 1848584560 C 18 48584593 C 18 48584602 ACT 18 48586262 C 18 48586291 G 1848591838 A 18 48591847 A 18 48591855 A 18 48591865 C 18 48593405 G 1848593465 G 18 48593475 T 18 48593495 A 18 48603032 C 18 48604682 A 1848604697 A 18 48604754 G 18 48604769 C Chromosome Position Alternate 177579801 C 17 37880220 C 17 37880261 T 17 37880981 AGCATACGTGATG (SEQ IDNO: 33) 17 37881332 A 17 37881378 G 17 37881440 T 18 48575112 C 1848575183 C 18 48575195 T 18 48575209 T 18 48575671 G 18 48581198 T 1848581229 A 18 48581243 T 18 48584560 T 18 48584593 T 18 48584602 A 1848586262 T 18 48586291 C 18 48591838 G 18 48591847 G 18 48591855 G 1848591865 G 18 48593405 C 18 48593465 A 18 48593475 TAC 18 48593495 G 1848603032 T 18 48604682 G 18 48604697 G 18 48604754 T 18 48604769 AChromosome Position Length Mutation ID Gene 17 7579801 1 gDNA35 TP53 1737880220 1 COSM14060 ERBB2 17 37880261 1 COSM1251412 ERBB2 17 3788098112 COSM20959 ERBB2 17 37881332 1 COSM14065 ERBB2 17 37881378 1 COSM686ERBB2 17 37881440 1 COSM21985 ERBB2 18 48575112 1 COSM1389031 SMAD4 1848575183 1 COSM14229 SMAD4 18 48575195 1 COSM218557 SMAD4 18 48575209 1COSM14168 SMAD4 18 48575671 1 COSM13115 SMAD4 18 48581198 1 COSM14118SMAD4 18 48581229 1 COSM1226725 SMAD4 18 48581243 1 COSM308153 SMAD4 1848584560 1 COSM14057 SMAD4 18 48584593 1 COSM22901 SMAD4 18 48584602 2COSM14217 SMAD4 18 48586262 1 COSM14163 SMAD4 18 48586291 1 COSM14167SMAD4 18 48591838 1 COSM1389054 SMAD4 18 48591847 1 COSM1389057 SMAD4 1848591855 1 COSM14109 SMAD4 18 48591865 1 COSM14111 SMAD4 18 48593405 1COSM14249 SMAD4 18 48593465 1 COSM14103 SMAD4 18 48593475 2 COSM14223SMAD4 18 48593495 1 AMXsynt12 SMAD4 18 48603032 1 COSM14096 SMAD4 1848604682 1 COSM14114 SMAD4 18 48604697 1 COSM1389099 SMAD4 18 48604754 1COSM14134 SMAD4 18 48604769 1 COSM1389106 SMAD4 Chromosome PositionMutation CDS 17 7579801 c.74 + 38C > G 17 37880220 c.2264T > C 1737880261 c.2305G > T 17 37880981 c.2324_2325ins12 17 37881332c.2524G > A 17 37881378 c.2570A > G 17 37881440 c.2632C > T 18 48575112c.306T > C 18 48575183 c.377T > C 18 48575195 c.389C > T 18 48575209c.403C > T 18 48575671 c.431C > G 18 48581198 c.502G > T 18 48581229c.533C > A 18 48581243 c.547C > T 18 48584560 c.733C > T 18 48584593c.766C > T 18 48584602 c.776_777delCT 18 48586262 c.931C > T 18 48586291c.955 + 5G > C 18 48591838 c.1001A > G 18 48591847 c.1010A > G 1848591855 c.1018A > G 18 48591865 c.1028C > G 18 48593405 c.1156G > C 1848593465 c.1216G > A 18 48593475 c.1229_1230insCA 18 48593495c.1246A > G 18 48603032 c.1333C > T 18 48604682 c.1504A > G 18 48604697c.1519A > G 18 48604754 c.1576G > T 18 48604769 c.1591C > A MutationTarget Sanger Chromosome Position Mutation AA Type Strand FrequencyDetection* 17 7579801 p.(=) SNV − genomic Not Covered 17 37880220p.L755S SNV + 5-15% Detected 17 37880261 p.D769Y SNV + 5-15% Detected 1737880981 p.A775_G776insYVMA INS + 5-15% Detected 17 37881332 p.V842ISNV + 5-15% Detected 17 37881378 p.N857S SNV + 5-15% Detected 1737881440 p.H878Y SNV + 5-15% Detected 18 48575112 p.P102P SNV + 5-15%Detected 18 48575183 p.V126A SNV + 5-15% Detected 18 48575195 p.P130LSNV + 5-15% Detected 18 48575209 p.R135* SNV + 5-15% Detected 1848575671 p.S144* SNV + 5-15% Detected 18 48581198 p.G168* SNV + 5-15%Detected 18 48581229 p.S178* SNV + 5-15% Detected 18 48581243 p.Q183*SNV + 5-15% Detected 18 48584560 p.Q245* SNV + 5-15% Detected 1848584593 p.Q256* SNV + 5-15% Detected 18 48584602 p.T259fs*4 DEL + 5-15%Detected 18 48586262 p.Q311* SNV + 5-15% Detected 18 48586291 p.? SNV +5-15% Detected 18 48591838 p.Q334R SNV + 5-15% Detected 18 48591847p.E337G SNV + 5-15% Detected 18 48591855 p.K340E SNV + 5-15% Detected 1848591865 p.S343* SNV + 5-15% Detected 18 48593405 p.G386R SNV + 5-15%Detected 18 48593465 p.A406T SNV + 5-15% Detected 18 48593475 p.Q410fs*6INS + 5-15% Detected 18 48593495 p.R416G SNV + 5-15% Detected 1848603032 p.R445* SNV + 5-15% Detected 18 48604682 p.R502G SNV + 5-15%Detected 18 48604697 p.K507E SNV + 5-15% Detected 18 48604754 p.E526*SNV + 5-15% Detected 18 48604769 p.R531R SNV + 5-15% Detected CHPv2TSACP TSTP Chromosome Position Detection Detection Detection 17 7579801Not Covered Not Covered Detected 17 37880220 Detected Detected NotCovered 17 37880261 Detected Detected Not Covered 17 37880981 DetectedNot Covered Detected 17 37881332 Detected Not Detected Not Covered 1737881378 Detected Detected Not Covered 17 37881440 Detected Detected NotCovered 18 48575112 Detected Not Covered Not Covered 18 48575183Detected Detected Not Covered 18 48575195 Detected Detected Not Covered18 48575209 Detected Detected Not Covered 18 48575671 Detected NotCovered Not Covered 18 48581198 Detected Detected Not Covered 1848581229 Detected Detected Not Covered 18 48581243 Detected Detected NotCovered 18 48584560 Detected Detected Not Covered 18 48584593 DetectedDetected Not Covered 18 48584602 Detected Detected Not Covered 1848586262 Detected Detected Not Covered 18 48586291 Detected Detected NotCovered 18 48591838 Detected Detected Detected 18 48591847 DetectedDetected Detected 18 48591855 Detected Detected Detected 18 48591865Detected Detected Detected 18 48593405 Detected Detected Not Covered 1848593465 Detected Detected Not Covered 18 48593475 Detected Detected NotCovered 18 48593495 Detected Detected Not Covered 18 48603032 DetectedDetected Not Covered 18 48604682 Detected Detected Detected 18 48604697Detected Detected Detected 18 48604754 Detected Detected Detected 1848604769 Detected Detected Detected Chromosome Position Reference 191207076 TG 19 1220321 T 19 1220371 G 19 1220382 C 19 1220487 G 191220502 G 19 1221293 C 19 1221319 C 19 1223125 C 19 3115012 C 19 3118942A 19 3119239 C 19 17945696 C 19 17948009 G 20 36031631 C 20 57480494 C20 57484420 C 20 57484596 A 22 24133967 C 22 24133990 C 22 24134006 C 2224143240 C 22 24145528 C 22 24145582 C 22 24145588 G 22 24145675 G 2224176353 GC Chromosome Position Alternate 19 1207076 T 19 1220321 C 191220371 T 19 1220382 T 19 1220487 T 19 1220502 T 19 1221293 T 19 1221319T 19 1223125 G 19 3115012 T 19 3118942 T 19 3119239 T 19 17945696 T 1917948009 A 20 36031631 T 20 57480494 T 20 57484420 T 20 57484596 T 2224133967 T 22 24133990 A 22 24134006 T 22 24143240 T 22 24145528CCCGAGGTGCTGGTCCCCAT (SEQ ID NO: 34) 22 24145582 T 22 24145588 A 2224145675 C 22 24176353 G Chromosome Position Length Mutation ID Gene 191207076 1 COSM21212 STK11 19 1220321 1 gDNA27 STK11 19 1220371 1COSM21570 STK11 19 1220382 1 COSM27316 STK11 19 1220487 1 COSM20944STK11 19 1220502 1 COSM25229 STK11 19 1221293 1 COSM29005 STK11 191221319 1 COSM21355 STK11 19 1223125 1 COSM21360 STK11 19 3115012 1COSM21651 GNA11 19 3118942 1 COSM52969 GNA11 19 3119239 1 gDNA28 GNA1119 17945696 1 COSM34213 JAK3 19 17948009 1 COSM34214 JAK3 20 36031631 1COSM1227526 SRC 20 57480494 1 COSM244725 GNAS 20 57484420 1 COSM27887GNAS 20 57484596 1 COSM27888 GNAS 22 24133967 1 COSM1002 SMARCB1 2224133990 1 COSM991 SMARCB1 22 24134006 1 COSM24595 SMARCB1 22 24143240 1COSM992 SMARCB1 22 24145528 19 COSM51386 SMARCB1 22 24145582 1 COSM993SMARCB1 22 24145588 1 COSM999 SMARCB1 22 24145675 1 gDNA30 SMARCB1 2224176353 1 COSM1057 SMARCB1 Chromosome Position Mutation CDS 19 1207076c.169delG 19 1220321 c.465 − 51T > C 19 1220371 c.465 − 1G > T 191220382 c.475C > T 19 1220487 c.580G > T 19 1220502 c.595G > T 191221293 c.816C > T 19 1221319 c.842C > T 19 1223125 c.1062C > G 193115012 c.547C > T 19 3118942 c.626A > T 19 3119239 c.771C > T 1917945696 c.2164G > A 19 17948009 c.1715C > T 20 36031631 c.1460C > T 2057480494 c.489C > T 20 57484420 c.601C > T 20 57484596 c.680A > T 2224133967 c.118C > T 22 24133990 c.141C > A 22 24134006 c.157C > T 2224143240 c.472C > T 22 24145528 c.566_567ins19 22 24145582 c.601C > T 2224145588 c.607G > A 22 24145675 c.601 + 66G > C 22 24176353 c.1148delCMutation Target Sanger Chromosome Position Mutation AA Type StrandFrequency Detection* 19 1207076 p.E57fs*7 DEL + 5-15% Detected 191220321 p.(=) SNV + genomic Not Covered 19 1220371 p.? SNV + 5-15%Detected 19 1220382 p.Q159* SNV + 5-15% Detected 19 1220487 p.D194YSNV + 5-15% Detected 19 1220502 p.E199* SNV + 5-15% Detected 19 1221293p.Y272Y SNV + 5-15% Detected 19 1221319 p.P281L SNV + 5-15% Detected 191223125 p.F354L SNV + 5-15% Detected 19 3115012 p.R183C SNV + 5-15%Detected 19 3118942 p.Q209L SNV + 5-15% Detected 19 3119239 p.T257TSNV + genomic Not Covered 19 17945696 p.V722I SNV − 5-15% Detected 1917948009 p.A572V SNV − 5-15% Detected 20 36031631 p.P487L SNV + 5-15%Detected 20 57480494 p.Y163Y SNV + 5-15% Detected 20 57484420 p.R201CSNV + 5-15% Detected 20 57484596 p.Q227L SNV + 5-15% Detected 2224133967 p.R40* SNV + 5-15% Detected 22 24133990 p.Y47* SNV + 5-15%Detected 22 24134006 p.R53* SNV + 5-15% Detected 22 24143240 p.R158*SNV + 5-15% Detected 22 24145528 p.L191fs*26 INS + 5-15% Detected 2224145582 p.R201* SNV + 5-15% Detected 22 24145588 p.A203T SNV + 5-15%Detected 22 24145675 p.(=) SNV + genomic Not Covered 22 24176353p.P383fs DEL + 5-15% Detected CHPv2 TSACP TSTP Chromosome PositionDetection Detection Detection 19 1207076 Detected Detected Detected 191220321 Detected Not Covered Detected 19 1220371 Detected Not CoveredDetected 19 1220382 Detected Not Covered Detected 19 1220487 DetectedDetected Not Covered 19 1220502 Detected Detected Not Covered 19 1221293Detected Detected Detected 19 1221319 Detected Detected Detected 191223125 Detected Detected Detected 19 3115012 Not Covered Detected NotCovered 19 3118942 Detected Detected Not Covered 19 3119239 Not CoveredDetected Not Covered 19 17945696 Detected Detected Not Covered 1917948009 Detected Detected Not Covered 20 36031631 Not Covered NotCovered Detected 20 57480494 Not Covered Not Covered Detected 2057484420 Detected Detected Detected 20 57484596 Detected Not Covered NotCovered 22 24133967 Detected Detected Not Covered 22 24133990 DetectedDetected Not Covered 22 24134006 Detected Detected Not Covered 2224143240 Detected Detected Not Covered 22 24145528 Not Detected NotCovered Not Covered 22 24145582 Detected Detected Not Covered 2224145588 Detected Detected Not Covered 22 24145675 Not Covered DetectedNot Covered 22 24176353 Detected Detected Not Covered

What is claimed is:
 1. A mixture of nucleic acid molecules comprising atleast one reference sequence and at least 15 variants of the at leastone reference sequence, wherein the nucleotide sequences of the at leastone reference sequence and each variant are defined prior to forming themixture, wherein each variant is at least 50% identical to the at leastone reference sequence, and wherein the variants comprise at least onesingle nucleotide polymorphism (SNP), multiple nucleotide polymorphisms(MNP), an insertion, a deletion, a copy number variation, a gene fusion,a duplication, an inversion, a repeat polymorphism, a homopolymer of theat least one reference sequence, and/or a nonhuman sequence.
 2. Themixture of nucleic acid molecules of claim 1, comprising at least 30variants.
 3. The mixture of nucleic acid molecules of claim 1, whereineach variant is related to cancer, an inherited disease, or aninfectious disease.
 4. The mixture of nucleic acid molecules of claim 1,wherein the nucleic acid sequence of each variant differs from itsneighbor variant by a predetermined percentage of 10% or less.
 5. Themixture of nucleic acid molecules of claim 1, wherein each variantcomprises a homopolymer sequence of at least 3 nucleotides.
 6. Themixture of nucleic acid molecules of claim 1, wherein each variantpossesses a nucleic acid barcode.
 7. The mixture of nucleic acidmolecules of claim 1, wherein each variant comprises a subsequence ofthe at least one reference sequence.
 8. The mixture of nucleic acidmolecules of claim 1, wherein the at least one reference sequence isselected from MPL, NRAS, ALK, MSH6, IDH1, ERBB4, VHL, MLH1, CTNNB1,FOXL2, PIK3CA, FGFR3, PDGFRA, KIT, KDR, FBXW7, APC, CSF1R, NPM1, EGFR,MET, SMO, BRAF, EZH2, FGFR1, JAK2, CDKN2A, GNAQ, ABL1, NOTCH1, RET,PTEN, FGFR2, HRAS, ATM, KRAS, PTPN11, HNF1A, FLT3, RB1, AKT1, IDH2,CDH1, TP53, ERBB2, SMAD4, STK11, GNA11, JAK3, SRC, GNAS, and SMARCB1. 9.A composition comprising the mixture of nucleic acid molecules of claim1, wherein each nucleic acid molecule is an oligonucleotide.
 10. Acomposition comprising the mixture of nucleic acid molecules of claim 1,wherein each nucleic acid molecule is a plasmid.
 11. The composition ofclaim 10, further comprising a cell wherein the plasmid is transfectedinto and/or mixed with the cell.
 12. The composition of claim 11,wherein the composition is formalin-fixed-paraffin embedded (FFPE) toproduce a FFPE sample.
 13. A composition comprising the mixture ofnucleic acid molecules of claim 1, wherein two or more of the nucleicacid molecules are on a single plasmid.
 14. The composition of claim 13,further comprising a cell wherein the plasmid is transfected into and/ormixed with the cell.
 15. The composition of claim 14, wherein thecomposition is formalin-fixed-paraffin embedded (FFPE) to produce a FFPEsample.
 16. A frequency ladder comprising the mixture of nucleic acidmolecules of claim 1, wherein the mixture is diluted to produce aplurality of variants at different frequencies.
 17. A frequency laddercomprising the mixture of nucleic acid molecules of claim 1, wherein themixture is diluted with the at least one reference sequence to produce aplurality of variants at different frequencies.
 18. A formalin-fixed,paraffin embedded (FFPE) sample composition comprising a cell, and aplasmid, wherein the plasmid is transfected into and/or mixed with thecell, and wherein the plasmid is a mixture of nucleic acid moleculescomprising at least one reference sequence and at least 15 variants ofthe at least one reference sequence, wherein the nucleotide sequences ofthe at least one reference sequence and each variant are defined priorto forming the mixture, wherein each variant is at least 50% identicalto the at least one reference sequence, and wherein the variantscomprise at least one single nucleotide polymorphism (SNP), multiplenucleotide polymorphisms (MNP), an insertion, a deletion, a copy numbervariation, a gene fusion, a duplication, an inversion, a repeatpolymorphism, a homopolymer of the at least one reference sequence,and/or a nonhuman sequence.